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Role & Responsibilities of Authorized Agent for Drugs in India (May 12, 2026)
How to Get a CDSCO Import License in India (Step-by-Step Guide (May 11, 2026)
Pharmacovigilance Regulations for Imported Drugs in India (May 6, 2026)
Inappropriate Use of AI in Pharmaceutical Manufacturing (May 1, 2026)
AI in Pharma Industry: Boon or Bane? Complete 2026 Guide (April 29, 2026)
CDSCO Cosmetic Import License India 2026 – Documents Checklist (April 13, 2026)
Regulatory Due Diligence for Medical Devices in India (March 31, 2026)
How to Apply for BIS Certification in India – Process, Documents & Timeline (March 23, 2026)
Regulatory Pathway for Biologicals in India – Approval Process & CDSCO Guidelines (March 23, 2026)
NDCT Amendment Rules 2026: Reduced Test License Approval Timelines (March 9, 2026)
NDCT Rules 2026: Permission or Prior Intimation for Test Licenses (March 9, 2026)
India EU FTA 2026: Tariffs, Market Access & Sector Impact (February 13, 2026)
FSSAI Standardised Risk Assessment Format from Jan 2026 (January 23, 2026)
FSSAI Compliance Checklist for Food Importers in India (January 21, 2026)
Medical Device Import Regulations in India: Step-by-Step (2025) (January 21, 2026)
Regulatory Due Diligence for Medical Devices: India & Global Market Guide | CliniExperts (December 5, 2025)
Top FAQs on CDSCO Medical Device Registration in India (November 3, 2025)
CDSCO Registration Timeline for Medical Devices in India (October 31, 2025)
How to Apply for CDSCO Medical Device Registration in India (2025 Guide) (October 22, 2025)
Surfing the Tariff Tsunami: Reinventing India’s Healthcare Exports (September 16, 2025)
FSSAI-Issued Consultation Paper on Compliance (July 28, 2025)
BIS Issues Guidance on Quality Control Orders (QCOs) (July 16, 2025)
What Does a Pharmaceutical Consultant Do? (June 30, 2025)
What are the three types of pharmacies? (June 30, 2025)
How can I join a pharma company? - CliniExperts (June 30, 2025)
What is the role of an IR consultant? (June 30, 2025)
How to become a pharmacometrician? (June 30, 2025)
How do I start a small consultancy? (June 30, 2025)
What are the 4 Ps of pharmacy? (June 30, 2025)
What is AAA in pharmacy? (June 30, 2025)
How to start a pharma consultancy? (June 27, 2025)
What does a Regulatory Consultant Do? (June 18, 2025)
Standards, Accreditation and Validity of FSSAI-Recognised Food Testing Laboratories - CliniExperts (June 4, 2025)
Organic Food Labelling In India| Certification, and Import of Organic Food in India - CliniExperts (April 21, 2025)
Cosmetic Label Compliance India | Cosmetic Product Registration and Labelling in India | (March 26, 2025)
Clinical Investigation Approvals Simplified: Understanding Forms MD-22 & MD-23 (January 15, 2025)
Regulatory Challenges of SaMD: A Guide to Global Standards and Compliance (November 4, 2024)
The Future of SaMD: Top Emerging Trends and Innovations in Medical Software (November 4, 2024)
Understanding SaMD: How Software Becomes a Regulated Medical Device (November 4, 2024)
Implementing Quality Management Systems for SaMD: A Guide to Compliance (October 22, 2024)
Clinical Validation of SaMD: Best Practices for Compliance and Innovation (October 22, 2024)
Types of FSSAI Licenses in Delhi: What You Need to Know (August 13, 2024)
Revised Schedule M: A Game Changer for Pharmaceutical Marketing (June 28, 2024)
Safety and Efficacy Assessment in Non-Specified Food Approval Across India (May 30, 2024)
FSSAI Advises all E-Commerce FBOs to De-link Miscategorized Beverages as “Health drinks/ Energy drinks” from Websites (April 25, 2024)
Wholesale Drug License Non Compliance Penalties (February 14, 2024)
Wholesale Drug License Registration Key Factors (February 14, 2024)
CPCB Alert - Timely Annual Report to be Submitted by PIBOs to Avoid Penalties (December 5, 2023)
Procedure to Meet the CDSCO License Mandate of Class C & D Non-Notified Medical Devices (October 25, 2023)
Legal Implications of the CDSCO License Update for Class C and Class D Medical Devices (September 4, 2023)
Purpose Of CDSCO SUGAM Portal Registration - Objective Of Online Sugam Portal Login (July 19, 2023)
Registration of Foreign Food Manufacturing Facilities (ReFoM) (May 2, 2023)
API Registration Of Drugs In India - Active pharmaceutical ingredient (April 28, 2023)
Summary On DTAB (Drug Technical Advisory Board), P1988 FDC’s (Fixed Dose Combinations) (April 17, 2023)
How to Apply for an FSSAI License / FSSAI Registration (April 4, 2023)
Import In-vitro Diagnostic for Sale or IVD for Distribution in India (February 21, 2023)
Manufacturing/import license for new Medical Devices / Permission to Import or Manufacture New Medical Device (February 13, 2023)
Benefits of the Wholesale Drug License - CliniExperts (February 2, 2023)
Wholesale Drug License Application Process - From, Fee and Required Documents (December 16, 2022)
Manufacture Class A-B Medical Devices - Forms, Fee, Validity, Timeline (October 31, 2022)
Integrated Pharmaceutical Database Management System 2.0 (IPDMS 2.0) and Pharma Sahi Daam 2.0 App Launched (October 20, 2022)
Medical Device Classification Pertaining to Hand-held Surgical Instruments for General surgical Procedures (October 10, 2022)
Test License for Medical Devices to Import - Checklist And Necessary Documents (September 21, 2022)
What is Form MD 7 & MD 9, and How To Apply for Class C & D Medical Device Manufacturing Permission? - CliniExperts (September 8, 2022)
ISO 13485 Medical Devices Certification: Medical Device ISO Standards (August 18, 2022)
Prevention of Consumers from Misleading Advertisements and Endorsements (August 5, 2022)
Draft of the new bill on New Drugs, Medical Devices and Cosmetics, 2022 - CliniExperts (July 28, 2022)
CLASS B MEDICAL DEVICE/IVD MANUFACTURING AND PRODUCT DEVELOPMENT SUPPORT (July 21, 2022)
Manufacturing And Product Development Support for Medical Devices / IVDs (Class C / D) (July 7, 2022)
Health Ministry Draft Notification To Add 16 Drugs as OTC Under Schedule K of Drugs Rules, 1945 - CliniExperts (July 4, 2022)
New Rules added by the CLA on suspension and cancellation of license of imported Medical Devices. - CliniExperts (June 22, 2022)
Manufacturing And Product Development Support For Class A Medical Devices/IVD’s - CliniExperts (June 20, 2022)
Medical Device Grouping as per MDR 2017 - CliniExperts (June 16, 2022)
CDSCO Update about regularization of rational fixed dose combinations (rational fdc) (May 13, 2022)
Medical Device Authorized Agent - Role & Responsibilities (April 14, 2022)
What Are The Cosmetic Regulations In India For Cosmetic License Approval? - CliniExperts (April 4, 2022)
What are CDSCO Form MD 26 and 27 and the benefits of having the import license for new medical devices? - CliniExperts (March 22, 2022)
How To Get Wholesale Drug Licenses In India? (March 8, 2022)
DCGI Classifies Medical Devices Pertaining To Rehabilitation (February 25, 2022)
Benefits Of Wholesale Drug License Form 20B & 21B / From 20B Drug License (February 15, 2022)
DCGI New Regulation For Cardiovascular Medical Devices Classification (February 8, 2022)
Why Do You Need In-Vitro Diagnostic Kits (IVD) Import License? (January 31, 2022)
DCGI New Regulation For Classification Of Medical Devices Pertaining Of Physical Support (January 17, 2022)
MoHFW Notification For Medical Devices Registration & Labelling, India (December 8, 2021)
CDSCO Recently Classified 80 In-Vitro Diagnostic Medical Devices For Regulation And Patient Safety - CliniExperts (October 27, 2021)
Drug Controller General of India (DCGI) Classifies 55 Medical Devices Pertaining to Dermatology and Plastic Surgery - CliniExperts (October 11, 2021)
DCGI Enlists New Regulation For The Classification Of Medical Devices Pertaining To Anesthesiology - CliniExperts (September 17, 2021)
Regulatory Updates on Disinfectants - CliniExperts (August 11, 2021)
COVID-19 Home Testing Using Rapid Antigen Tests (RATs) - CliniExperts (June 10, 2021)
CDSCO Provides Guidelines For Approval Of COVID-19 Vaccines For Restricted Use In An Emergency Situation In India And For The Import Of Vaccine By The Private Sector - CliniExperts (June 2, 2021)
Extended Timelines For Submission Of Notarized/ Apostilled Documents For Import And Registration Of Cosmetics - CliniExperts (May 31, 2021)
CDSCO Orders Regulation Of CT Scan Equipment, All Implantable Devices, Medical Equipment As Drugs - CliniExperts (May 31, 2021)
CDSCO Notifies To Update The Product Insert Of 4th Generation HIV In-Vitro Diagnostics Kit - CliniExperts (April 22, 2021)
CDSCO codifies New Cosmetics Rules,2020 - CliniExperts (April 2, 2021)
Regulation of 4 Medical Devices as Drugs by CDSCO: A new Notification - CliniExperts (March 10, 2021)
Notification For Ultrasound Equipment From CDSCO: Extension Of Timeline - CliniExperts (January 5, 2021)
CDSCO releases the timeline for Regularization of Rational Fixed Dose Combination in India - CliniExperts (December 3, 2020)
New classifications of non-notified medical devices and IVDs in India by CDSCO (November 9, 2020)
CDSCO Releases Draft Regulatory Guidelines For The Development Of Vaccines In COVID-19 Pandemic (October 26, 2020)
Classification Of Non-Notified Medical Devices By CDSCO (October 19, 2020)
CDSCO Releases Notice For The Online Application Of Certificates Of Notified Devices (September 18, 2020)
Relaxation Of Drug License For Selling And Stocking Hand Sanitizers (September 10, 2020)
CliniExperts Aided The Faster Approval Of Edinburgh Genetics Colloidal Gold Immunoassay And Whole Blood Collection COVID-19 Kits - CliniExperts (September 2, 2020)
Accelerated Approval Of RealCycler CORO-G Real Time PCR Kits By CliniExperts - CliniExperts (September 2, 2020)
CDSCO Notified Information On Convalescent Plasma In COVID-19 - CliniExperts (August 20, 2020)
CDSCO extends timeline for Import of Drugs with residual shelf life less than 60 percent till Oct 31 (August 20, 2020)
RCGM And CDSCO Recommends Fast Track Processing Of Recombinant Vaccines Applications For COVID-19 - CliniExperts (June 26, 2020)
Ethics Committee Guidance amid COVID-19 Pandemic in India (June 12, 2020)
What should you know about manufacturing licenses for new API and formulations in India? (June 12, 2020)
Biocan Launches Rapid Antibody Test Kits For Novel Coronavirus (COVID-19) (June 1, 2020)
Regulatory Approvals And Pathway For The Manufacture Of Ventilators Amid COVID-19 - CliniExperts (May 25, 2020)
The Indian Ministry of Consumer Affairs Relaxes Import Norms of Infrared Thermometers - CliniExperts (April 29, 2020)
Usage of Personal Protective Equipment rationally during COVID-19 Pandemic (April 28, 2020)
Notice for release of Consignments of Vaccines and In-vitro Diagnostics in COVID-19 Pandemic (April 22, 2020)
CliniExperts Facilitating Fast Track Approval of COVID-19 Diagnostic Kits in India (April 14, 2020)
CDSCO Announced Clinical Trials Conduct Rules During COVID-19 Outbreak - CliniExperts (April 13, 2020)
Regulations for Hand sanitizers and home drug deliveries by CDSCO in India (April 6, 2020)
New Notification on Regulating All Devices – Deciphering the Key Concepts - CliniExperts (March 31, 2020)
Deciphering The Medical Devices Amendment Rules 2020 - CliniExperts (March 27, 2020)
CDSCO prioritizes Regulatory Approval of In-vitro Diagnostic Kit for COVID-19 - CliniExperts (March 27, 2020)
New Regulatory Guidance to Facilitate Drug & Vaccine Approval for COVID-19 - CliniExperts (March 27, 2020)
CDSCO Releases Frequently Asked Questions on Import and Registration of Drugs in India (November 7, 2019)
New Regulation Introduced in Cosmetics Industry (July 30, 2019)
Regulatory Changes in India - Be in Control of Compliance (July 23, 2019)
Consumer Safety through Cosmetics Labeling Regulation - What’s New? (July 19, 2019)
Addressing Regulatory Compliance of Cosmetics Manufacturing & Sales in India (July 15, 2019)
How recent Regulatory changes will impact Cosmetics Registration in India? (July 11, 2019)
Introducing Safety in Cosmetics Usage through Regulatory Reforms (July 8, 2019)
New Rules for Clinical Trials and Drugs Promote Research and Ensure Patient Safety (May 30, 2019)
Draft of New Regulations for Clinical Trials in India Favours Drug Development in the Country (May 9, 2019)
New Regulations of Government of India Considers 8 Medical Devices as Drugs (March 29, 2019)
New Notice by DCGI for Medical Devices (January 2, 2019)
Licenses Required For Operating a Smart Watch Business in India - Part 2 (October 9, 2018)
Marketing Authorization of Biological Products in India (September 26, 2018)
How Legal Metrology Affects the Market of Smart Watches - Part 1 (September 17, 2018)
Licensing Process and Rules Related to Phytopharmaceutical Drugs in India (September 4, 2018)
Phytopharmaceutical Drugs and Their Related Regulations in India (August 22, 2018)
Legal Metrology - Importer Registration, Dealer License, Repair License, Manufacturing License (August 6, 2018)
CASE STUDY: Facilitator at a Indo-German Medical Device Conclave (July 27, 2018)
Legal Metrology Packaged Commodity Rules 2017 (July 25, 2018)
Marketing Authorization of Insecticides in India (July 2, 2018)
Update on Food Safety and Standards (Labelling and Display) Regulations Draft, 2018 (June 6, 2018)
Comparison of Initial Draft and Final Gazette Regulations for Alcoholic Beverages (June 4, 2018)
Legal Metrology - Importer, Manufacturer and Packaging Registration (June 1, 2018)
Expected Changes in FSSAI Labeling Regulations and Gazetted Alcoholic Beverage Regulations (May 30, 2018)
New Regulations for Medical Devices Industry by CDSCO | CliniExperts (December 23, 2017)
Self-Assessment/Audit of Unit for GMP/GLP Compliance (November 3, 2017)
Principles for Safety & Performance of Medical Devices (November 1, 2017)
Kokate Committee - History, Constitution, & Action Plan (July 5, 2017)
New Medical Device Rules To Be Rolled Out In 2018 (April 20, 2017)
FSSAI Regulations for Caffeinated Beverages (January 20, 2017)
Medical Devices Rules 2017 - Medical Device Regulations, Classification, And Registration (January 9, 2017)
India Champions e-Governance for Pharma Industry (December 29, 2016)
Medical Device Registration in India, Call +91 7672005050 (November 29, 2016)
Draft Guidelines on Similar Biologics, 2016 (November 24, 2016)
FSSAI Draft Norms for E-Commerce FBO's (November 10, 2016)
Sugam Portal - CDSCO Sugam Registration / Login Support (October 10, 2016)
Health Supplement FSSAI License, Regulatory Guidelines for Proprietary Food in India (September 26, 2016)
Initiatives on Global Clinical Trials (September 7, 2016)
Coronary Stents included in NLEM (September 7, 2016)
Faster Import of Human Biological Samples (September 7, 2016)
Subject Expert Committee’s Updates (August 30, 2016)
Top Five Trends Changing the Game in Global Healthcare IT - CliniExperts (August 3, 2016)
NDAC/MDAC/SEC - CliniExperts (July 29, 2016)
Clinical Trial - CliniExperts (July 29, 2016)
Summary of New Drug, New FDC and SND as per Drug and Cosmetic Act - CliniExperts (July 29, 2016)
Global Licensing & Registration - CliniExperts (July 28, 2016)
Global Drug & Medical Device Regulatory Consulting - CliniExperts (July 28, 2016)
Insecticide Registration - CliniExperts (July 28, 2016)
State FDA & Zonal CDSCO - CliniExperts (July 28, 2016)
Consultation on Medical Device and Diagnostic Kit for India Market - CliniExperts (July 28, 2016)
CLINICAL TRIAL ON MEDICAL DEVICE - CliniExperts (July 28, 2016)
APPLICATION TO MARKET NEW CHEMICAL ENTITIES (NCEs) - CliniExperts (July 28, 2016)
APPLICATION TO MARKET NEW CHEMICAL ENTITIES (NCEs) - CliniExperts (July 28, 2016)
ANCILLARY CARE TO THE CLINICAL TRIAL SUBJECTS - CliniExperts (July 28, 2016)
Import NOC for import of small quantity of cosmetics - CliniExperts (July 28, 2016)
Labeling of Cautionary Note under Rule of 97 of Drug & Cosmetic Act – (No. DCGI/MISC/572012) - CliniExperts (July 28, 2016)
Govt forms panels to frame guidelines & SOPs for approval of new drugs, trials, banning drugs - CliniExperts (July 28, 2016)
First amendment in Drugs & Cosmetics Rules 2013 - CliniExperts (July 28, 2016)
EC Registration Support - CliniExperts (July 28, 2016)
Submission of PSUR - CliniExperts (July 28, 2016)
Cosmetics Registration - CliniExperts (July 28, 2016)
Cosmetic Regulatory Strategy Consulting & Liaison Delhi, India - CliniExperts (July 27, 2016)
Cosmetic Products Submission & Approval in Delhi, India - CliniExperts (July 27, 2016)
Cosmetic Products Marketing & Import Regulation in India - CliniExperts (July 27, 2016)
Cosmetic License Application & Registration in India - CliniExperts (July 27, 2016)
Test licence for import of small quantity of drugs to be obtained from Zonal office, CDSCO - CliniExperts (July 14, 2016)
Clarification and requirements related to Post approval changes as per CDSCO Guidance for Industry for Biological Products - CliniExperts (July 14, 2016)
Guidelines on “Similar Biologics: Regulatory requirements for Market Authorization in India” will be implemented from 15th September 2012. - CliniExperts (July 14, 2016)
Fourth Amendment in Drugs & Cosmetics Rules, 2013 - CliniExperts (July 14, 2016)
NDAC meeting Support - CliniExperts (July 14, 2016)
Cosmetic Regulations, Registration and Import Registration in India - CliniExperts (July 13, 2016)
Indian Cosmetic Regulation Webinar By Dr. Ashwini Kumar - CliniExperts (July 13, 2016)
Cosmetic Regulation in India - CliniExperts (July 12, 2016)
First pill To Prevent HIV - Only For Some Patients (July 12, 2016)
FSSAI Compliance Services, Leading FSSAI License Consultant in India (July 12, 2016)
MEDICAL WRITING - CliniExperts (July 12, 2016)
REQUIREMENT OF LOCAL TRIAL FOR A GENERIC OR BIO-SIMILAR IN OTHER COUNTRY LIKE USA FOR ITS APPROVAL IN THE COUNTRY - CliniExperts (August 10, 2014)
FBO must adhere to FSSAI guidelines, published on website of regulator - CliniExperts (August 8, 2014)
FSSAI extends food licensing, registration deadline to February 4, 2015 - CliniExperts (August 5, 2014)
FIXED DOSE COMBINATION OF FLUPENTHINOL & MELITRACEN BANNED FOR HUMAN USE. - CliniExperts (July 12, 2014)
A Blueprint for Helping Children with Rare Diseases - CliniExperts (July 10, 2014)
WAIVER OF CLINICAL TRIAL FOR NEW DRUG APPROVAL IN INDIAN PATIENTS - CliniExperts (July 10, 2014)
LIMITING NUMBER OF CLINICAL TRIALS AN INVESTIGATOR CAN UNDERTAKE - CliniExperts (July 10, 2014)
Drug Controller General of India to pharma MNCs: Conduct fruitful clinical trials for Indians - CliniExperts (July 9, 2014)
COMPENSATION FOR CLINICAL TRIAL IN CASE OF INJURY OR DEATH DISCERNED AT A LATER STAGE - CliniExperts (July 5, 2014)
Keeping You Informed: An Update on FDA’s Judicious Use Strategy for Antimicrobial Drugs in Food-Producing Animals - CliniExperts (July 1, 2014)
FDA Refines Its Thinking on Nanotechnology - CliniExperts (June 29, 2014)
Narendra Modi govt plans to clip wings of drug regulator - CliniExperts (June 24, 2014)
Import of Cosmetics Tested On Animal Prohibited - CliniExperts (May 21, 2014)
CDSCO has drafted guidelines for determining Quantum of financial compensation to be paid in case of Clinical Trial related Injury or Death - CliniExperts (April 25, 2014)
Second Amendment in Drugs & Cosmetics Rule, 2013 - CliniExperts (September 2, 2013)
Third Amendment in Drugs & Cosmetics Rules, 2013 - CliniExperts (July 10, 2013)
Import of small quantities of cosmetics - CliniExperts (July 5, 2013)
Government bans sale and manufacture of pain killer Dextropropoxyphene - CliniExperts (May 24, 2013)
Notification for Cosmetic Registration in India - CliniExperts (March 30, 2013)
Notification for the Submission of Safety and Efficacy of FDC permitted to manufacture but not approved by DCGI - CliniExperts (January 10, 2013)
Clarification For Import Of Non-Notified Medical Devices - CliniExperts (January 9, 2013)
Guidelines on Registration of Import of Cosmetics - CliniExperts (January 2, 2013)
DCGI to meet zonal officials to re-examine regulatory requirement for vaccines - CliniExperts (November 26, 2012)
Pfizer, Bristol get EU nod for blood clot preventer - CliniExperts (November 21, 2012)
10 Shocking Medical Mistakes - CliniExperts (November 6, 2012)
Ginger muscles in on diabetes - CliniExperts (August 7, 2012)
Sleep centers provide lessons for need to adapt in changing health system - CliniExperts (July 31, 2012)
First pill to prevent HIV is only for some patients - CliniExperts (July 31, 2012)
CDSCO has made it mandatory for Ethics Committee to get registered so as to get authority to review and accord its approval to Clinical Trial protocol - CliniExperts (July 28, 2012)
Gene that spreads breast cancer discovered paving the way for new treatments - CliniExperts (July 26, 2012)
Heartburn pills taken by millions 'can increase risk of cancer and heart disease' - CliniExperts (July 26, 2012)
Heartburn pills taken by millions ‘can increase risk of cancer and heart disease - CliniExperts (July 25, 2012)
Novartis Wins U.S. Approval for Afinitor in Breast Cancer - CliniExperts (July 21, 2012)
Diabetes drug costing just 2p could beat prostate cancer by shrinking tumours - CliniExperts (July 16, 2012)
FDA Approves First New Weight-Loss Pill In Decade - CliniExperts (June 27, 2012)
A Supreme Court split decision will cause health confusion - CliniExperts (June 7, 2012)

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    - Biological Authorized Agent Support / Biologicals Registration Holder Support For Biologics (April 21, 2022)
    - Biological Import License for Drugs | Permission To Import Biological License (January 27, 2022)
    - Biological Registration Certificate For Importer Form 40, 41/ Biological Regulatory Services (December 31, 2021)
    - Permission for Clinical Trial & GCT for Importer (June 2, 2016)
    - India Regulatory Services > Biologicals Import License (June 2, 2016)
    - India Regulatory Services > Biologicals - Registration for Importers (June 2, 2016)
  - India Regulatory Services > Biologicals For Manufacturers (June 24, 2016)
    - Get Your Test License to Manufacture Biologicals In India with Ease (June 7, 2024)
    - NOC for form 29 - Clarification Letter For Biological Manufacturers (May 17, 2024)
    - Biologicals Marketing Authorization Approval in India | Biologics Regulatory Requirements for Marketing Authorization (April 18, 2024)
    - CDSCO Manufacturing License for Biologicals in India (March 7, 2024)
    - Permission For Clinical Trial Phase 1, 2, 3 In India – CT 04 and CT 06 (February 12, 2024)
    - Marketing Authorization (Form 44, Form 46) For Manufacturers (June 2, 2016)
    - Permission for Clinical Trial & GCT for Manufacturer (June 2, 2016)
    - Biologicals Post Approval Changes For Manufacturers (June 2, 2016)
- IVD Regulatory Consultants in India - In Vitro Diagnostics IVD Regulatory Services (March 31, 2016)
  - Achieve An EPR Authorization Certificate From CPCB For E-Waste Management (October 17, 2024)
  - How to Get EPR authorization certificate from CPCB For Battery in India (October 14, 2024)
  - EPR Authorization Certificate Guide: Forms I, V, VI & VII for CPCB in India (September 19, 2024)
  - Permission To Conduct Clinical Performance Evaluation Of In-Vitro Diagnostic Kit India (August 12, 2022)
  - Non-notified IVD Registration | Non-notified In Vitro diagnostic Approval in India For Importer/Manufacturer (July 28, 2022)
  - In-Vitro Diagnostic Kit ISO 13485 Certification Assistance / ISO Consultant For IVD (June 27, 2022)
  - In-Vitro Diagnostic Kits Label Compliance, IVD Labeling Requirements, In Vitro Diagnostic Device Labeling Requirements (April 29, 2022)
  - Clarification Letter / No Objection Certificate For In-Vitro Diagnostic Kit (February 21, 2022)
  - India Regulatory Services > Diagnostic Kit > Risk Based Classification (August 27, 2018)
  - India Regulatory Services > New In-Vitro Diagnostic First Time in India (August 27, 2018)
    - Permission to Import/Manufacture New In-Vitro Diagnostic which does not have a Predicate Kit (Form MD-29) (August 27, 2018)
    - Permission to Conduct Clinical Performance Evaluation for New In-Vitro Diagnostic (Form MD-25) (August 27, 2018)
  - Performance Evaluation from NIB (June 24, 2016)
  - Clarification Regarding Diagnostic Kits from CDSCO (June 24, 2016)
  - India Regulatory Services > Diagnostic Kit For Manufacturers (June 24, 2016)
  - India Regulatory Services > In Vitro Diagnostic Kit For Importers (June 24, 2016)
    - Permission For Import Predicate IVD Kit License CDSCO Form Md 14 15 (February 29, 2024)
    - Retention of IVD Import License | Renewal of in-vitro diagnostic kit license for importer (September 20, 2023)
    - Permission to Import In vitro Diagnostic Kit Test License for Clinical Investigation | IVD Test License For Importers (MD 16 & MD 17) (August 12, 2022)
    - Post Approval Changes For In-Vitro Diagnostic Kits | IVD Post Approval Services In India (June 14, 2022)
    - Permission For In Vitro Diagnostic Kit Test License | IVD Test License (March 22, 2022)
    - Authorized Agent Support For In-vitro Diagnostic Kit | IVD Registration Support (February 14, 2022)
    - Import License For IVD (In-Vitro Diagnostic Kits) CDSCO Form MD14, 15 (December 15, 2021)
    - Permission for Import License (Form MD-14, Form MD-15) (June 2, 2016)
    - Permission for Test License to Import In-Vitro Diagnostic Kit (Form MD-16, Form MD-17) (June 2, 2016)
    - Test License (Form 11) | Diagnostic Kit for Importers (June 2, 2016)
    - Registration of Notified Diagnostic Kits for Importers (June 2, 2016)
    - Authorized Agent/ Registration Holder | Diagnostic Kit (June 2, 2016)
- Medical Device Regulatory Consultants in India | Medical Device Regulatory Services (March 31, 2016)
  - UKCA Regulatory Due Diligence for Medical Devices (September 23, 2025)
  - US Regulatory Due Diligence for Medical Devices (September 23, 2025)
  - Australia Regulatory Due Diligence for Medical Devices | Cliniexperts (September 16, 2025)
  - Canada Regulatory Due Diligence for Medical Devices (September 16, 2025)
  - Due Diligence for Medical Devices (September 3, 2025)
  - E-waste EPR Registration Post compliance In India | EPR Compliance For E-Waste (March 7, 2024)
  - EPR Authorization Certificate from CPCB | Apply For EPR Certificate Online (February 26, 2024)
  - Registration of Class a Non-sterile and Non-measuring Medical Device (March 24, 2023)
  - PC PNDT Act / PC-PNDT Certificate / PCPNDT License - Pre conception Pre natal Diagnostic Technique Certificate (September 27, 2022)
  - Permission To Conduct Clinical Investigation License, Medical Device Clinical Performance Evaluation Form MD 22 23 (July 28, 2022)
  - Sugam Registration For Medical Devices; In-Vitro Diagnostic Kits Sugam License, Medical Device IVD Sugam Approval (May 10, 2022)
  - Medical Device Label Compliance, Medical Device Labeling Requirements For Medical Devices Compliance (April 29, 2022)
  - Medical Device ISO 13485 Certification: Make strides Quality and Compliance. (March 2, 2022)
  - Medical Device Clarification Letter Or No Objection Certificate For Medical Devices (NOC) (February 21, 2022)
  - Non-notified Medical Devices Registration To Import/Manufacture In India (January 18, 2022)
  - Investigational New Device/ New Device - First Time In India (June 5, 2018)
    - Manufacture/Import New Medical Devices Permission / License India - CDSCO Form MD-26, MD-27 (December 9, 2021)
    - Permission to Import/Manufacture Medical Device which does not have a Predicate Device (June 5, 2018)
    - Permission to Conduct Clinical Investigation for Investigational Medical Device (Form MD-23) (June 5, 2018)
  - Assistance on MDAC Meeting for Medical Devices (June 24, 2016)
  - Clarification Regarding Medical Devices from CDSCO (June 24, 2016)
  - Medical Device Regulations For Manufacturers (June 24, 2016)
    - Retention Of Loan License To Manufacture Medical Device - Loan License Retention For Medical Devices (June 14, 2023)
    - Retention of Medical Device Manufacturing License For Class C- D, Medical Device Manufacturing License Retention Consultant (June 14, 2023)
    - Permission To Manufacture Class C D Medical Devices Services In India – From MD 7 MD 9 (June 6, 2022)
    - Permission To Manufacture Class A B Medical Devices (Form MD 3, MD 5) (May 9, 2022)
    - Permission For Test License To Manufacture Medical Devices - Form MD 12, MD 13 (March 22, 2022)
    - Free Sale Certificate For Medical Devices | Medical Device FSC Certification (March 22, 2022)
    - Loan License To Manufacture Medical Devices Class A B - Medical Device Loan License Approval (March 22, 2022)
    - Loan License To Manufacture Medical Devices Class C D | Medical Device Loan License (March 22, 2022)
    - Permission for Test License to Manufacture Medical Device (Form MD-12, Form MD-13) (June 2, 2016)
    - Permission to Manufacture or Permission for loan license to manufacture Class C & D Medical Device (Form MD-9, Form MD-10) (June 2, 2016)
    - Permission to Manufacture / Permission for Loan License to Manufacture Class A & B Medical Device (Form MD-5 and Form MD-6) (June 2, 2016)
  - Medical Device Regulations For Importers (June 24, 2016)
    - WPC License, WPC Approval, ETA Consultant | WPC Certificate For Import (July 11, 2022)
    - Post Approval Changes Medical Products | Medical Device Post Approval Services In India (June 14, 2022)
    - Authorized Agent Support For Medical Device | Medical Device Authorized Representative (February 2, 2022)
    - Permission To Import Medical Devices Test License | Test License to Import Medical Device (January 6, 2022)
    - Permission To Import Medical Devices License India | Medical Device Import Form MD14 MD15 (December 1, 2021)
    - Marketing Authorization for New Medical Device (Form 44 & 45) (June 2, 2016)
    - Amendments in Registration Certificate for Medical Devices (June 2, 2016)
    - Import License for Medical Devices (Form 10) (June 2, 2016)
    - Permission For Test License To Import Medical Device (Form MD-16, Form MD-17) (June 2, 2016)
    - Authorized Agent/ Registration Holder for Medical Device (June 2, 2016)
- Cosmetics Regulatory Services - Cosmetic Registration Process, Permission, License In India (March 31, 2016)
  - Cosmetics Label Compliance, Cosmetics Labeling Rules Requirements (May 10, 2022)
  - Permission To Import New Cosmetics | License to Manufacture New Cosmetics Form Cos 3 (February 22, 2022)
  - Labeling Assistance - CliniExperts (July 21, 2016)
  - Cosmetic Sample Testing (June 24, 2016)
  - Cosmetic For Manufacturer, Cosmetic Manufacturing License | Permission to Manufacture Cosmetics (June 24, 2016)
    - Cosmetic Manufacturing License (June 2, 2016)
  - Cosmetic Registration Certificate In India - Cosmetic License For Importer (Cos-1, Cos-2) (June 24, 2016)
    - Post Approval Changes For Cosmetics | Cosmetics Post Approval Services In India (July 11, 2022)
    - Cosmetics Authorized Agent Support / Registration Holder Support For Cosmetics (April 20, 2022)
    - Endorsement (October 30, 2020)
    - Heavy metals with respect to cosmetics - CliniExperts (October 7, 2020)
    - Schedule S (September 18, 2020)
    - BIS Standards with Respect to Cosmetics (September 16, 2020)
    - Endorsement of Cosmetics - CliniExperts (March 13, 2019)
    - List of documents for cosmetics - CliniExperts (March 4, 2019)
    - Compliance with Respect to Cosmetics (March 4, 2019)
    - List of Cosmetics Products - All Cosmetic Products Name List (March 4, 2019)
    - BIS Standards with Respect to Cosmetics (March 4, 2019)
    - Re-registration of Cosmetic Products, Renewal of of Cosmetic Products (June 2, 2016)
    - Amendment in Cosmetic Registration Certificate (June 2, 2016)
    - Cosmetic Registration and Approval (Form 42, 43) (June 2, 2016)
    - Cosmetic Authorized Agent/ Registration Holder Support (June 2, 2016)
- FSSAI Consultants - Food Regulatory Services In India | FSSAI Food License Registration (March 31, 2016)
  - Simplify Your FSSAI License Renewal in India Process (July 30, 2024)
  - How To Obtain A Sanitary Import Permit For Livestock And Products (July 29, 2024)
  - FSSAI Annual Return Filing In India (Form D1) – Online Food Business Return Filing (February 5, 2024)
  - FSSAI Registration of Foreign Food Manufacturing Facilities (ReFoM) in India (January 18, 2024)
  - Apply for Modification of FSSAI License / Registration – FSSAI Food License Modification (January 18, 2024)
  - FSSAI Food Compliance For Food Supplements Nutraceuticals - Food Product Compliance (January 17, 2023)
  - FSSAI Advertisement Claim Approval - Food Supplements & Nutraceuticals Claim Approval (January 2, 2023)
  - Food Supplements License / Fssai Registration For Nutraceuticals In Form C (December 19, 2022)
  - FSSAI Approval for non-specified Food Supplements & Nutraceuticals Regulation (November 15, 2022)
  - FSSAI Food Claim Approval, Fssai Claim Approval, FSSAI Products Approval, Food Ingredient approval (July 28, 2022)
  - FSSAI Authorized Agent Support, Food Registration Holder Support Or Authorized Representative (April 19, 2022)
  - FSSAI Compliance Services, Food Product Compliance Requirements (April 8, 2022)
  - FSSAI License Apply Online | FSSAI Registration Consultants In India - FSSAI Food License (January 18, 2022)
  - FSSAI Non-Specified Food Product Approval | Non-Specified Food Ingredient License (January 17, 2022)
  - Food Import License Holder (July 21, 2016)
  - FSSAI Product Approval Consultant (June 24, 2016)
  - Food Licensing and Registration (June 24, 2016)
  - India Regulatory Services > Food Import Assistance (June 24, 2016)
- Drug Regulatory Consultants, Drug Regulatory Services, Online Drug License Registration (March 31, 2016)
  - India Regulatory Services > Drug for Importer (June 24, 2016)
    - Advanced Shelf Life Extension Solutions for Your Products (June 7, 2024)
    - How to Obtain an Import License for Drugs in India Form 8/8A & 10/10A (May 28, 2024)
    - Permission of Repacking Under Rule 37 of Drugs & Cosmetics Act, 1940 (May 1, 2024)
    - Drug Re-registration for Importer in Form 40 - Renewal of Drug Registration Certificate (April 18, 2024)
    - Test License To Import Drugs | Permission For Drug Import Test License (November 2, 2022)
    - Post Approval Changes To Drug Substances | Drug Post Approval Services (June 1, 2022)
    - Authorized Agent Support For Drugs / Drugs Registration Holder Support (February 15, 2022)
    - Drug registration certificate For Importer | Registration Certificate For Import Of Drugs In India (June 2, 2016)
    - Drug Marketing Authorization Approval in India | New Drug Regulatory Requirements for Marketing Authorization (June 2, 2016)
    - Authorized Agent/Registration Holder Support | Drug for Importers (June 2, 2016)
  - India Regulatory Services > Drug For Manufacturer (June 24, 2016)
    - Good Manufacturing Practices for Pharmaceuticals (May 26, 2025)
    - Pharmaceutical And Compliance Services Made Simple: Reliable Solutions (November 22, 2024)
    - Manufacture Unapproved API For Development of Formulation for Test / Analysis / CT / BA / BE in India – CT 15 (February 5, 2024)
    - New Drug Approval Process in India | Procedure For Approval of New Drug (NDA) (October 9, 2023)
    - Manufacture Formulation Of Unapproved API Drugs | Unlock The Potential Of Unapproved API Drugs (September 25, 2023)
    - Test License To Manufacture Drugs | Permission For Drug Manufacturing Test License (November 2, 2022)
    - Wholesale Drug License Form 20B 21B - Drugs Distributor / Wholesale License Registration (December 31, 2021)
    - Drug Test License | Drug for Manufacturer (June 2, 2016)
    - Free Sales Certificate (June 2, 2016)
    - Form 29 for Test Batch (June 2, 2016)
    - Permission For Drug Manufacturing License – Drug Manufacturer License Approval Process (June 2, 2016)
    - Dual NOC from CDSCO (June 2, 2016)
    - Medical Writing Services for Drug Manufacturer (June 2, 2016)
    - Clinical Trials in India | Regulatory Requirements, Phases & Approval Process (June 2, 2016)
    - Bioequivalence (BE) Studies (June 2, 2016)
    - Toxicity Studies for Drug Manufacturers (June 2, 2016)
    - Subject Expert Committee (SEC) Meetings (June 2, 2016)
    - Export NOC, Special Code Neutral Code For NOC (June 2, 2016)
    - BE NOC for Export (Bioequivalence NOC for Drugs) (June 2, 2016)
    - Subsequent New Drug Approval (SND) | Subsequent New Drugs Application (June 2, 2016)
    - New Drug Approval (NDA) (June 2, 2016)
    - Investigational New Drug (IND) Application – CT NOC For Investigational New Drugs (June 2, 2016)

News Feed

The Story Behind CliniExperts: From Regulatory Gap to Stronger Systems (April 16, 2026)
Drug and Medical Device Regulatory Dynamics in India (June 16, 2025)
CliniExperts Recognized by CBIC for Exceptional GST Compliance in FY 2023-24 (July 26, 2024)
Most Promising Medical Device Device & Pharmaceutical Regulatory Consultant From Asia (September 5, 2023)
Healthcare Budget 2023-24 gets its deserved due Insights from CliniExperts CEO - CliniExperts (February 2, 2023)
CliniExperts and vCare Denmark come together for inclusive and holistic Regulatory Solutions (September 23, 2022)
CliniExperts - The go-to-team for India's healthcare regulatory affairs management - India Today - CliniExperts (June 16, 2022)
CliniExperts - The Multidisciplinary Regulatory Solution Provider - Forbes - CliniExperts (April 4, 2022)
Industry Outlook Magazine Recognised CliniExperts on its Cover Story, under the Top Ten Healthcare Regulatory Service Providers List-2022 - CliniExperts (February 2, 2022)
The Economic Times recognizes Dr. Ashwini Kumar, CEO CliniExperts Services Pvt. Ltd. for exemplifying the spirit of Entrepreneurial passion - CliniExperts (July 2, 2020)
CliniExperts: India’s First Healthcare Regulatory Solutions Provider For Domestic And International Markets - CliniExperts (April 10, 2019)
Express Pharma: In the Quest of True Freedom - CliniExperts (August 20, 2018)
CliniExperts : Unmatched Regulatory Consultants in India- CIO Reviews- June 2014 - CliniExperts (July 14, 2016)
Silicon India- Dec. 2015 Editorial (Page 8 and Page 22) - CliniExperts (July 14, 2016)
A special feature – Companies invest in R&D to tap future opportunities- Chronicle Pharmabiz- August 7, 2014 - CliniExperts (July 13, 2016)
CliniExperts: Unmatched Regulatory Consultants in India - CliniExperts (July 13, 2016)

Testimonials

India Regulatory Expert Series

Authorized Agent Support For Medical Devices - CliniExperts (September 7, 2023)
Medical Device and IVD Import License/Approval in India - CliniExperts (September 7, 2023)
New Cosmetics Rule 2020 For Cosmetics Product Registration - CliniExperts (September 7, 2023)
Indian Cosmetic Regulation Webinar - CliniExperts (October 10, 2022)

Regulatory Updates

Corrigendum/Addendum Dated 4.5.2026 in the Guidelines under PLI Scheme for Bulk Drugs - CliniExperts (May 11, 2026)
Direction under Section 16(5) of Food Safety and Standards Act, 2006 regarding enforcement of the new standards for Meat Sausages notified under Food Safety and Standards (Food Products Standards and Food Additives) First Amendment Regulations, 2025 - CliniExperts (May 7, 2026)
Monitoring the Sale of Fresh Fruits for the Use of Unauthorized or Prohibited Artificial Ripening Agents - CliniExperts (May 7, 2026)
Draft Food Safety and Standards (Packaging) Amendment Regulations, 2026, regarding the inclusion of the list of packaging materials for pan masala - CliniExperts (May 7, 2026)
Amendment to the Uniform Code for Marketing Practices in Medical Devices 2024 -regarding - CliniExperts (May 7, 2026)
Implementing the process for prior approval and risk assessment through the single window system (ePAAS) - CliniExperts (May 7, 2026)
CDSCO Notice on Disposal/Rejection of Long Pending Applications on SUGAM Portal (May 6, 2026)
Fees for verification of weights and measures by the Government Approved Test centres approved under the Legal Metrology Government Approved Test Centre Rules, 2013- reg. - CliniExperts (May 5, 2026)
Draft Notification to the Food Safety and Standards (Packaging) Regulation, 2018 for inclusion of list of packaging material for Pan Masala - CliniExperts (May 1, 2026)
Press Note - 23-04-2026 - Special Enforcement Drive - Weight Loss Drugs - CliniExperts (April 29, 2026)
LM PC Second Amendment Rules 2026 (April 29, 2026)
Fixation of Ceiling prices for Scheduled formulations under revised Schedule -I (NLEM 2022) of DPCO 2013 notified vide S.O. No. 5249 dated 11.11.2022 - CliniExperts (April 28, 2026)
G.S.R. 299(E): Draft Rule 89 Amendment for Form 29 Licenses (2026) (April 27, 2026)
COVID-19 Vaccines Approved in India as on 22.04.2026 (April 27, 2026)
System improvement in Payment workflow for visual inspection and laboratory testing charges in FICS/SWIFT to enhance ease of doing business - CliniExperts (April 22, 2026)
CDSCO Form CT-05 Prior Intimation System for Export Studies (April 22, 2026)
CDSCO G.S.R. 270(E): Draft Medical Devices Rules Amendments (April 21, 2026)
2026.04.10_G.S.R. 269(E)_Draft Notification to amend certain provisions w.r.t. Medical Device Testing Fee under MDR, 2017 - CliniExperts (April 21, 2026)
FSSAI Advisory: Non-Use of Ashwagandha Leaves in Food Products (April 17, 2026)
Safety of Household, Commercial & Similar Electrical Appliances (April 13, 2026)
Notification for revision in ceiling prices of 6 scheduled formulations under NLEM 2011 based on WPI - CliniExperts (April 7, 2026)
OM regarding Movement in Wholesale Price Index (WPI) for the preceding calendar year 2025 over the year 2024 - CliniExperts (April 7, 2026)
Food Safety and Standards (Labelling and Display) First Amendment Regulations, 2026 relating to exemption of RDA in case of Infant nutrition products, Non-retail containers etc - CliniExperts (April 7, 2026)
Draft notification of Food Safety and Standards (Food Products Standards and Food Additives) Amendment Regulations, 2026 for substitution of the reference of “Food Safety and Standards (Packaging and Labelling) Regulations, 2011" with “Food Safety and Standards (Labelling and Display) Regulations, 2020" and “Food Safety and Standards (Packaging) Regulation, 2018 - CliniExperts (April 7, 2026)
SCO IVF Medical Devices Licensing Update 2026 | IUI Kits & ART Devices Compliance (April 2, 2026)
FAQs on Food Safety and Standards (Licensing and Registration of Food Businesses) Amendment Regulations, 2026 - CliniExperts (April 2, 2026)
Notification for revision in ceiling prices of 138 scheduled formulations under NLEM 2015 based on WPI - CliniExperts (April 1, 2026)
Notification for revision in ceiling prices of 767 scheduled formulations under NLEM 2022 based on WPI - CliniExperts (April 1, 2026)
Advisory to all manufacturers, importers and marketing authorization holders - CliniExperts (April 1, 2026)
Online Applications for Post Approval Changes (PAC) w.r.t Marketing Authorization (MA) for r-DNA products - CliniExperts (April 1, 2026)
CDSCO Dossier-Based Drug Licensing | Compliance & ONDLS (April 1, 2026)
GSR 164(E) Blood Product Testing Draft Rule 2026 (March 27, 2026)
Implementation of ‘Food Recall’ functionality under Food Safety Compliance System (FoSCoS) - CliniExperts (March 27, 2026)
Compliance obligations of E-commerce FBOs in the context of Open Network for Digital Commerce model - CliniExperts (March 27, 2026)
MoHFW Approves Major Regulatory Reforms to Promote Ease of Doing Business and Strengthen Food Safety Framework - CliniExperts (March 27, 2026)
Objections or suggestions, if any, may be addressed to the Chief Executive Officer, Food Safety and Standards Authority of India, FDA Bhawan, Kotla Road, New Delhi- 110002 or sent on email at regulation[at]fssai[dot]gov[dot]in - CliniExperts (March 27, 2026)
Advisory regarding mandatory registration/license by Milk Producers (other than members of dairy cooperative societies) / Milk Vendors - CliniExperts (March 27, 2026)
Food Safety and Standards (Licensing and Registration of Food Businesses) Amendment Regulations, 2026 - CliniExperts (March 27, 2026)
Online Applications for grant of license in Form 28-D/28-DA for r-DNA products - CliniExperts (March 26, 2026)
Unapproved Drug Alert: Sodium Hyaluronate Eye Drops 0.3% (March 26, 2026)
Legal Metrology Third Amendment Rules 2026 (March 23, 2026)
G.S.R. 173(E) Draft Notification – Drugs Rules Amendment (March 23, 2026)
Transfer of certain functions and delegation of powers to the zonal offices of CDSCO under Rule 22 of the Drugs and Cosmetics Rules, 1945 - CliniExperts (March 18, 2026)
FSSAI Turnover Threshold 2026: New License Rules Explained (March 16, 2026)
FSSAI CEO Calls for Nationwide Crackdown on High-Risk Food Commodities at 49th CAC Meeting - CliniExperts (March 12, 2026)
In exercise of the powers conferred by sub-clause (b) of clause (xi) of section 2 of the Narcotic Drugs and Psychotropic Substances Act, 1985 (61 of 1985), the Central Government hereby declares the following substances, salts and preparations thereof to be manufactured drugs, namely: - CliniExperts (March 12, 2026)
CDSCO Prior Intimation System for CT-10, CT-12 & CT-13 (March 11, 2026)
2026.02.18 S.O. 912(E)_Notification of Medical Device Testing Officers (MDTO) for Laboratories - CliniExperts (March 11, 2026)
FSSAI Organises First FoSTaC Training Programme for Street Food Vendors in East Delhi - CliniExperts (March 11, 2026)
CBN Registration Certificate (CRC) Under NDPS Rules 1985 (March 9, 2026)
Special festive drive to ensure food safety, quality and prevention of adulteration for upcoming Holi festival - CliniExperts (March 9, 2026)
Compliance to provisions of FSS (Recognition and Notification of the laboratories) Regulations 2018 by FSSAI recognized Laboratories - CliniExperts (March 9, 2026)
GSR 135(E) Drugs Rules 2026: Rule 121A & License Updates (March 2, 2026)
Reduction in the Maximum Retail Price (MRP) on account of reduction/exemption from Custom duty - CliniExperts (March 2, 2026)
Legal Metrology General Second Amendment Rules 2026 Update (February 21, 2026)
LM packaged commodities amendment rules 2026 - CliniExperts (February 20, 2026)
Doxycycline related CNS Side Effects (Restlessness, Anxiety, Irritability, Nervousness, and Dizziness) - Recommendations for the change in Prescribing Information Leaflets (PILs) - CliniExperts (February 20, 2026)
Carbimazole related agranulocytosis - Recommendations for the change in Prescribing Information Leaflets (PILs) - CliniExperts (February 20, 2026)
Draft Guidance document for Import of In-vitro diagnostic Medical device for stakeholders comment (dated 30.01.2026) - CliniExperts (February 19, 2026)
Strengthening Adverse Event Reporting under the Materiovigilance Programme of India (MvPI) – Compliance by Medical Device Marketing Authorisation Holders - CliniExperts (February 17, 2026)
FSSAI Launches Comprehensive Online Training Programme on Food Safety Risk Assessment - CliniExperts (February 13, 2026)
Objections or suggestions, if any, may be addressed to the Chief Executive Officer, Food Safety and Standards Authority of India, FDA Bhawan, Kotla Road, New Delhi- 110002 or sent on email at regulation[at]fssai[dot]gov[dot]in - CliniExperts (February 13, 2026)
Direction under Section 16(5) of Food Safety and Standards Act, 2006 regarding enforcement of the new standards for Meat Sausages notified under Food Safety and Standards (Food Products Standards and Food Additives) First Amendment Regulations, 2025 - CliniExperts (February 13, 2026)
2026.01.22 G.S.R. 52(E)_Draft Notification for Revision of testing fees under Schedule B and B1 - CliniExperts (February 12, 2026)
2026.02.02 G.S.R. 98(E)_Draft Notification regarding amendment in NDCT Rules, 2019 for Omit the requirements of granting of Provisional Certificate for registration of ethics committee - CliniExperts (February 12, 2026)
2026.02.02 G.S.R. 97(E)_Draft Notification regarding submission of post approval changes in NDCT, Rules 2019 - CliniExperts (February 12, 2026)
2026.01.28 G.S.R. 66(E)_Draft Notification for consideration of Navi Mumbai International Airport (NMIA) as authorized Airport for Drug Import, under the provision of Rule 43A of Drugs Rules 1945 - CliniExperts (February 12, 2026)
2026.01.21 G.S.R. 54(E)_Draft Notification for amendment in Schedule H1 for inclusion of Pregabalin and its drug formulations - CliniExperts (February 12, 2026)
2026.01.20 G.S.R. 45(E)_ Draft Notification for exemption of Animal Toxicity Studies w.r.t. certain conditions - CliniExperts (February 10, 2026)
Draft Rule Mandates Blue Line Label for Antimicrobial Drugs (February 5, 2026)
CDSCO Rejects Long-Pending SUGAM Applications Awaiting Replies (February 2, 2026)
CDSCO Updates Authorized Labs for IVD Performance Evaluation (February 2, 2026)
NDCT Amendment Rules 2026: Test License Changes GSR 46(E) (January 29, 2026)
Decision taken in 48th Food Authority meeting related to ‘Policy regarding timeline for the compliance of FSS Regulation - CliniExperts (January 29, 2026)
Compounding of Offences under the Drugs and Cosmetics Act, 1940 in accordance with the Drugs and Cosmetics (Compounding of Offences) Rules, 2025 - CliniExperts (January 21, 2026)
Guidelines on Compounding of Offences under the Drugs and Cosmetics Act, 1940 as per Drugs and Cosmetics (Compounding of Offences) Rules, 2025 - CliniExperts (January 20, 2026)
Legal Metrology Amendment Rules 2026: BP Monitor Standards (January 16, 2026)
Risk classification list of medical devices pertaining to Oncology - CliniExperts (January 8, 2026)
2025.12.29_G.S.R. 927(E)_Draft notification for Removal of Syrup exemption under schedule K - CliniExperts (January 7, 2026)
Draft Rules on the Legal Metrology Government Approved Test Centre Amendment Rules, 2026 for comments from stakeholders - CliniExperts (January 5, 2026)
2025.12.29_ S.O. 6091(E)_Notification regarding Nimesulide above 100 mg in immediate release dosage form - CliniExperts (January 5, 2026)
Implementation of Standardized Format for submission of representation seeking risk assessment - CliniExperts (January 2, 2026)
Notification of Manufacturers under Rule 54 of NDPS Rules, 1985 (Effective for the period upto 31st December, 2027) - CliniExperts (January 2, 2026)
New provision for Risk Classification of Medical Devices on the CDSCO Online System for Medical Devices - CliniExperts (December 30, 2025)
FSSAI Clarification on Use of the Word “Tea” in Food Labels (December 30, 2025)
Compliance of Scheme of Testing for Packaged Drinking Water & Mineral Water - CliniExperts (December 30, 2025)
MoHFW issues Draft Amendment to Medical Device Rules 2017: GSR 883(E) (December 24, 2025)
MedTech Mitra IVD Innovators Handbook: ICMR & CDSCO Guide (December 24, 2025)
Legal Metrology General 7th Amendment Rules 2025 Explained (December 24, 2025)
NDPS Amendment Rules 2025: Form 4A & Form 5 Changes (December 24, 2025)
Display of QR Code at retail/wholesale pharmacies across the country to report Adverse Drug Reactions to PvPI - CliniExperts (December 22, 2025)
NPPA has fixed retail prices of 11 formulations under Drugs (Prices Control) Order, 2013 based on the decision of 140th Authority meeting dated 27.11.2025 - CliniExperts (December 16, 2025)
Food Safety and Standards (Alcoholic Beverages) Second Amendment Regulations, 2025 - CliniExperts (December 10, 2025)
Enforcement Action Against Use of Industrial Dye Auramine in Food Products such as Roasted Chana and Other Product - CliniExperts (December 10, 2025)
LM packaged commodities second amendment rules 2025 - CliniExperts (December 9, 2025)
Requirement of License issued by CDSCO/State Licensing Authorities in procurement of Medical Devices by procurement agencies - CliniExperts (December 9, 2025)
The Legal Metrology (General) Sixth Amendment Rules, 2025. - Breath Analyser - CliniExperts (December 8, 2025)
Advisory on availability of Rapid Testing Kits for Milk/Milk products Vending/Kiosk machines operated by Dairy Units - CliniExperts (November 26, 2025)
FSSAI and CBIC Go Live with SWIFT 2.0 Pilot to Enhance Transparency and Efficiency in Food Imports - CliniExperts (November 24, 2025)
Ceiling Prices of Orthopaedic Knee Implants for Knee Replacement System based on the decision of 139th Authority meeting dated 14.11.2025 - CliniExperts (November 24, 2025)
Withdrawal of Tin Ingot (Quality Control) Order, 2025 - CliniExperts (November 21, 2025)
Machinery and Electrical Equipment Safety (Omnibus Technical Regulation) Second Amendment Order, 2025 - CliniExperts (November 21, 2025)
Draft Food Safety and Standards (Alcoholic Beverages) Amendment Regulations, 2025 relating to standards for special wine - CliniExperts (November 13, 2025)
Hydroxymethylfurfural (HMF) to be considered as a quality parameter in Honey - CliniExperts (November 13, 2025)
Legal Metrology FAQs | Key Compliance Clarifications 2025 (November 12, 2025)
NPPA has ceiling price fixation of 06 scheduled formulations of Schedule-I (NLEM 2022) under Drugs (Prices Control) Order,2013 based on decision of the 138th Authority meeting dated 30.10.2025 - CliniExperts (November 12, 2025)
NPPA has fixed retail prices of 28 formulations under Drugs (Prices Control) Order, 2013 based on the decision of 138th Authority meeting dated 30.10.2025 - CliniExperts (November 12, 2025)
Advisory on Environmentally Compliant Disposal of Seized, Rejected and Expired Food Items - CliniExperts (November 12, 2025)
Food Safety and Standards (Import) First Amendment Regulations, 2025 relating to Method of Analysis and Signing Authority - CliniExperts (November 12, 2025)
Risk-Based Classification List of Class A Medical Devices (Non-Sterile, Non-Measuring) | CDSCO Update (November 11, 2025)
CDSCO G.S.R. 810(E) Corrigendum on BA/BE Studies Sample Size 2025 (November 11, 2025)
Post Approval changes for clinical trials (Form CT-06) for CGTP through SUGAM Online Portal - CliniExperts (November 7, 2025)
CEO, FSSAI Urges States/UTs to Strengthen Consumer Grievance Mechanism and Proactively Highlight Enforcement Actions - CliniExperts (November 4, 2025)
8th Session of Codex Committee on Spices and Culinary Herbs (CCSCH) inaugurated in Guwahati - CliniExperts (November 4, 2025)
Provision for Granting Registration Certificate for Seasonal Food Businesses - CliniExperts (November 4, 2025)
CDSCO Draft Guidance on Medical Device Software under MDR 2017 (November 3, 2025)
CBN Public Notice: Additional Opium & Codeine Allocation 2025 (November 3, 2025)
G.S.R. 760(E): Restrictions on Alcohol-Based Drug Products (November 3, 2025)
G.S.R. 758(E): CLAA Amendment for Cell & Gene Therapies (November 3, 2025)
G.S.R. 759(E): Draft Rules on Liquid Antiseptic Regulation (November 3, 2025)
G.S.R. 757(E) Amendment: New Categories Added to Schedule H2 (November 3, 2025)
Digital Monitoring System on the ONDLS portal for monitoring the supply chain of high-risk solvents - CliniExperts (October 30, 2025)
Draft Legal Metrology Packaged Commodities Second Amendment Rules, 2025 for comments from stakeholders reg - CliniExperts (October 30, 2025)
The Legal Metrology Packaged Commodities Amendment Rules, 2025 dated 24.10.2025 - CliniExperts (October 30, 2025)
The Legal Metrology Government Approved Test Centre Amendment Rules, 2025 - CliniExperts (October 30, 2025)
Draft Food Safety and Standards (Packaging) Amendment Regulations, 2025 regarding provisions related to Poly- and perfluoroalkyl substances (PFAs) and Bisphenol A (BPA) for food contact materials - CliniExperts (October 30, 2025)
Withdrawal of Orders regarding "Usage of the term ORS along with brand names" dt 14.10.2025 - CliniExperts (October 30, 2025)
Clarification regarding Order dated 14.10.2025 on withdrawal of permissions for use of the term “ORS” along with brand names - CliniExperts (October 23, 2025)
Circular to all State/UT Licensing Authorities regarding recent revised GST rate Structure - CliniExperts (October 16, 2025)
Notice for inviting comment to ensure a level playing field in new drug approval in India - CliniExperts (October 16, 2025)
Strict compliance with the Drugs Rules 1945 for testing of raw materials and finished formulations - CliniExperts (October 16, 2025)
Mapping of ICEGATE with CDSCO-Notified Ports - CliniExperts (October 16, 2025)
Global Food Regulators Summit 2025 concludes in New Delhi with a joint resolve to strengthen International Collaboration and build Inclusive Food Safety Frameworks - CliniExperts (October 13, 2025)
Union Health Minister Shri J P Nadda Inaugurates the Third Edition of Global Food Regulators Summit 2025 - CliniExperts (October 13, 2025)
FSSAI and Department of Agriculture, Fisheries and Forestry, Australia signs MoU in the area of food safety - CliniExperts (October 13, 2025)
Enforcement Drive on Spices (Whole & Powder) to be kept in abeyance until further orders - CliniExperts (October 13, 2025)
FSSAI Launches Licensing Framework for manufacturing of Ayurveda Aahara on FoSCoS Portal - CliniExperts (October 10, 2025)
Processing of Grant of WHO GMP COPP applications in respect of products under consideration for license approval through ONDLS Portal - CliniExperts (October 9, 2025)
Tin Ingot (Quality Control) Amendment Order, 2025 - CliniExperts (October 9, 2025)
2025.09.23_S.O. 4338(E)_prohibit the import, manufacture, sale and distribution of certain antimicrobial products for animal use - CliniExperts (October 9, 2025)
Special festive drive to ensure food safety, quality and prevention of adulteration during the month of September-October, 2025 - CliniExperts (October 6, 2025)
Clarification for grant of permission for combipack product of lyophilised dry powder for injection /I.V infusion and diluents for reconstitution such as sterile water for injection / sodium Chloride Injection - CliniExperts (October 3, 2025)
Enforcement Drive on Spices (Whole & Powder) for the Month of October, 2025 - CliniExperts (October 3, 2025)
Clarification for regulatory pathway for Cocrystals - CliniExperts (September 30, 2025)
Ceiling Prices of Orthopaedic Knee Implants for Knee Replacement System based on the decision of 137th Authority meeting dated 15.9.2025 - CliniExperts (September 30, 2025)
NPPA has fixed retail prices of 9 formulations under Drugs (Prices Control) Order, 2013 based on the decision of 137th Authority meeting dated 15.9.2025 - CliniExperts (September 30, 2025)
Frequently Asked Questions on GST Part-1 - CliniExperts (September 29, 2025)
Frequently Asked Questions on GST Part-3 - CliniExperts (September 29, 2025)
GST FAQs Part 2 | Clarifications on Medicines, Services & Goods (September 26, 2025)
GST Revised Price Sticker Permission | Legal Metrology Rules 2011 (September 23, 2025)
ICMR CDSCO Protocols IVD Kits | Standard Performance Evaluation 2025 (September 23, 2025)
Subsequent Importer Medical Devices | CDSCO Online Provision 2025 (September 22, 2025)
MRP Revision GST Updated Directions | NPPA & CDSCO 2025 (September 22, 2025)
MRP Revision GST Rates Effective 22 Sept 2025 | NPPA Update (September 22, 2025)
GST Medical Product Sticker Permission | CDSCO Update 2025 (September 18, 2025)
Extension of separate ceiling price under Para 11(3) w.r.t IV Fluids based on the decision of 136th Authority meeting dated 28.8.2025 - CliniExperts (September 18, 2025)
Extension of separate ceiling price under Para 11(3) w.r.t other IV Fluids based on the decision of 136th Authority meeting dated 28.8.2025 - CliniExperts (September 18, 2025)
NPPA has fixed retail prices of 42 formulations under Drugs (Prices Control) Order, 2013 based on the decision of 136th Authority meeting dated 28.8.2025 - CliniExperts (September 18, 2025)
Shri Rajit Punhani, IAS, takes charge as CEO, FSSAI - CliniExperts (September 16, 2025)
Introduction of new Kind of Business (KoB) for Ayurveda Aahara under FoSCoS for License/Registration - CliniExperts (September 16, 2025)
Braille Labeling Medicines: Public Comments Invited | CDSCO 2025 (September 15, 2025)
Revised MRP GST Permission for Unsold Stock | Legal Metrology Update 2025 (September 12, 2025)
Legal Metrology Model Approval Draft Amendment 2025 | Public Comments Invited (September 12, 2025)
Approved FDC Voglibose Metformin HCl SR 500 mg | CDSCO Corrigendum 2025 (September 11, 2025)
IBSC Approval CT-10 Accepted for Test Item Manufacturing | CDSCO 2025 (September 11, 2025)
Inviting comments on standard IVD evaluation protocols drafted by ICMR and CDSCO - CliniExperts (September 2, 2025)
Government Revises Enforcement Timeline for Machinery and Electrical Equipment Safety Regulation - CliniExperts (August 1, 2025)
Extension of Deadline for WHO GMP COPP Applications via ONDLS Portal - CliniExperts (August 1, 2025)
Clinical Trial for cell and gene therapeutic products is online - CliniExperts (August 1, 2025)
Legal Metrology Package Commodities Rules and Legal Metrology Act (June 15, 2025)
CDSCO Releases Updated List of Laboratories for Performance Evaluation of IVD Medical Devices - CliniExperts (June 13, 2025)
Clarification on Labeling Permissions under Rule 104A of Drugs and Cosmetics Rules, 1945 - CliniExperts (May 31, 2025)
Guidelines on Disposal of Expired/Unused Drugs - CliniExperts (May 31, 2025)
Guidelines for acceptance of recycled Polyethylene terephthalate (PET) as Food Contact Material (FCM-rPET) - CliniExperts (May 31, 2025)
Discontinuation of the Term "100%" on Food Product Labels and Related Promotional Materials (May 31, 2025)
Unapproved/Approved New Drugs Manufacturing NoC for Export Purposes - CliniExperts (May 20, 2025)
Long awaited revamp of Revised Guidelines on Similar Biologics- Regulatory requirements for Marketing Authorization (May 16, 2025)
Public Notice on Regulation of Export of Codeine Phosphate Preparations (May 16, 2025)
Refined Zinc (Quality Control) Order, 2025 (May 7, 2025)
Refined Nickel (Quality Control) Order, 2025. - CliniExperts (May 7, 2025)
Primary Lead (Quality Control) Order, 2025. - CliniExperts (May 7, 2025)
Introduction of Auto‑Generated MSC and NCC for Licensed Medical Devices - CliniExperts (April 23, 2025)
Regulatory Update on Examination of 2nd Assessment Report by Prof. Kokate Committee - CliniExperts (April 18, 2025)
New Online System for Auto-generated Neutral Codes for Export under Medical Devices Rules, 2017 - CliniExperts (April 18, 2025)
Regulatory Update on Unapproved Fixed Dose Combinations (FDCs) - CliniExperts (April 18, 2025)
CDSCO Transitions to Automated Online System for Issuance of MSC and NCC for Medical Devices - CliniExperts (April 16, 2025)
Addendum to FAQ on Medical Devices Rules, 2017 - CliniExperts (April 16, 2025)
CDSCO Issues Guidelines for Transfer of Drugs from SEZ to Domestic Tariff Area - CliniExperts (April 16, 2025)
CDSCO Proposes Risk Classification Changes for Cardiovascular and Neurological Devices (April 8, 2025)
CDSCO Enables MSMEs to Apply Online Extension On Revised Schedule M (March 30, 2025)
FSSAI Vegan Foods Amendment Regulations 2025 – What Importers Must Know (March 12, 2025)
Regulatory Update: New Format for Quarterly Returns on Psychotropic Substances (March 12, 2025)
CRO Registration On SUGAM Portal & Renewal – Everything You Need to Know (March 12, 2025)
CDSCO Export NOC Process Guide – How to Obtain Approval for New Drugs (March 12, 2025)
New Drugs NDCT Rules 2019: Gastro-Resistant & Delayed-Release Drugs (March 8, 2025)
Clinical Trial Site Addition & PI Change: Simplified Process via Sugam Portal (March 8, 2025)
CDSCO FDC Application Deadline: Submit FDC Applications by May 2025 (March 7, 2025)
Draft IVD-MD Adverse Event Reporting Form Open for Comments (March 7, 2025)
FSSAI Mandatory Update of Form IX & Auto-Approval for Non-Form C in FoSCoS (March 2, 2025)
Ban Nimesulide For Animal Use: New Government Notification Explained (March 1, 2025)
FSSAI Draft Labelling Rules 2025: Public Feedback & Key Updates (February 26, 2025)
Legal Metrology Amendment 2025: New Labeling Rules for Medical Devices (February 26, 2025)
Drugs Amendment Rules 2025: Implementation of Schedule M (February 22, 2025)
CDSCO Introduces Additional Variant Module on SUGAM Portal for Cosmetics (February 21, 2025)
New Legal Metrology Rules for IST 2025 – Public Consultation Open Now (February 14, 2025)
CCPA’s Greenwashing Guidelines: Effective Date & Compliance Rules (February 7, 2025)
Legal Metrology Rules, 2011: Latest Amendments 2024 (February 7, 2025)
Schedule M Compliance Extension for Small & Medium Drug Manufacturers (February 5, 2025)
New FSSAI Rule: Food Labeling Changes to Be Enforced Annually on July 1st (February 5, 2025)
Legal Metrology Test Centre Rules: Key Amendments & Regulatory Updates (February 5, 2025)
ICMR’s 2025 Guidance on Rapid Diagnostic Validation & AST (February 4, 2025)
Implementation Timeline for Medical Device Classification Amendments (February 4, 2025)
Risk-Based Classification of Medical Devices & IVDs in India (February 4, 2025)
2025 Quota Allocation of Narcotics Drugs: Guidelines and Application Steps (January 14, 2025)
Food Safety E-Commerce FBOs: Explore Key compliance requirements (January 14, 2025)
Simplified Process for Clinical Trial Site Addition and PI Changes on SUGAM Portal (January 14, 2025)
Why FSSAI Requires Quarterly Data on Expired and Rejected Food Items (January 14, 2025)
Immediate Prohibition of Nimesulide for Animal Use by Ministry of Health (January 14, 2025)
Food Safety and Standards (Amendment) Rules, 2024: Essential Changes and Their Impact (December 18, 2024)
FSSAI Notifies NABL-Accredited Lab for Testing Prohibited Substances in Food (December 18, 2024)
FSSAI Tightens Oversight: Packaged Water Designated High-Risk Food (December 18, 2024)
FSSAI's New Standards for Mozzarella Cheese and Neera: Enhanced Food Safety Regulations (November 14, 2024)
Food Safety Regulations Amended by the FSSAI: Prohibition and Restrictions on Sales (November 14, 2024)
Complete Guide to Medical Device Adverse Event Reporting in India for Manufacturers (November 14, 2024)
New FSSAI 2011 Regulations: Strick Limits Of Contaminants and toxins (November 14, 2024)
CDSCO Enforces Online Applications for Veterinary Drug Approvals in India (October 16, 2024)
New CDSCO Restrictions: Limit on Number of Products Per SUGAM Application For Cosmetics (September 11, 2024)
Understanding Schedule M And WHO TRS Guidelines For Pharma Manufacturers (September 4, 2024)
Central Government Bans Etodolac + Paracetamol Combination: Full Guidance (September 4, 2024)
FSSAI Prohibits Non-Specified Ingredients in Fruit Juices Without Prior Approval (August 10, 2024)
Latest FoSCoS Update For Direct Sellers: New Business Models And Guidelines. (August 1, 2024)
Re-operationalisation of Draft FSS Regulations: What You Really want to Be aware in 2024 (July 4, 2024)
FSSAI Enforces Removal of claim of 100% Fruit Juices from Labels and ads. (July 3, 2024)
Comprehensive Guidance For Industry On Pharmacovigilance For Human Vaccines (June 11, 2024)
Essential Guide to Registration Of Laboratory For Medical Device Manufacturer (June 11, 2024)
Lifetime License Certificate of Manufacture or Import of Medical Devices (May 21, 2024)
Strategies to Minimize Adverse Effects of Medical Devices (May 21, 2024)
Import/manufacture Regulations for Class C & D Medical Devices (May 21, 2024)
Clarification for E-Commerce FBOs on Categorization of Health Drinks and Energy Drinks (April 10, 2024)
Submission of online applications of PSURs w.r.t Marketing Authorization(MA) of New Drugs/ SNDs/ FDCs/ Biologicals/ Veterinary Reg. (March 12, 2024)
Cosmetics Rules 2020 in Form Cos-4A - Annual details of cosmetics imported by the applicant (March 8, 2024)
CDSCO Launches Online Neutral Code Application for Manufacturing of Medical Devices (February 21, 2024)
CDSCO Launched Additional Forms on National Single Window System (NSWS) Portal (February 2, 2024)
Drugs (Amendment) Rules 2023 - Schedule M of Drugs Rules, 1945 - CliniExperts (January 12, 2024)
CDSCO Launched National Single Window System (NSWS) Portal (January 4, 2024)
CDSCO and ICMR Launches MedTech Mitra (January 4, 2024)
Post Approval Changes (PAC) Applications for Marketing Authorization (MA) for Human Vaccines and Anti-sera (December 5, 2023)
FSSAI extends operationalization of FSS Regulations 2022 (November 30, 2023)
Products with S-Adenosyl-L-Methionine (SAMe) are not considered Food Products (November 10, 2023)
License Applications for Class C and D Medical Devices deemed valid for upto 6 months (November 10, 2023)
Combination Package, Group Package and Multi-piece Package introduced in Legal Metrology (Packaged Commodities) Amendment Rules 2023 - CliniExperts (October 28, 2023)
Government seeks public feedback on the Prevention and Regulation of Dark Patterns 2023 (September 27, 2023)
Import / Export of six unregulated chemicals (September 9, 2023)
Online Test licence for Veterinary Vaccines / Drugs (August 10, 2023)
Bar Code or QR Code Implementation on Top 300 Brands (August 10, 2023)
Regulations on Legal Metrology (Packed Commodities) Rules, 2011 for Medical Devices (August 8, 2023)
Amendment of the Legal Metrology Packaged Commodities Rules (July 11, 2023)
14 Fixed Dose Combination Drugs (FDCs) Are Prohibited by Central Ministry of India (June 14, 2023)
Operationalization of MRL - Maximum Residue Limit of Pesticides used in Tea by FSSAI (May 26, 2023)
FSS Advertising and Claims - Food Safety and Standards Advertising & Claims Regulations, 2018 (May 26, 2023)
Re-operationalisation of FSS Regulations for Health Supplements, Nutraceuticals, prebiotic and Probiotic Food (May 26, 2023)
Launch of the unified online portal by the Central Bureau of Narcotics (CBN) - CliniExperts (May 24, 2023)
Class C Class D Medical Devices Regulatory Update | Non-notified Medical Devices Regulatory Update (April 28, 2023)
16 Fixed Dose Combinations (FDCs) Evaluation by DTAB Sub-Committee (April 18, 2023)
Quality And Safety Of Nutraceuticals And Health Supplements (April 11, 2023)
Frequently Asked Questions on application for vegan logo endorsement FAQs (March 18, 2023)
New Food Safety and Standards For Food Products and Food Additives (March 18, 2023)
Traceability Application under Repurpose Used Cooking Oil (RUCO) initiative (March 18, 2023)
Extension of Requirement of Health Certificate with Import of Food Consignment (March 17, 2023)
Guidelines for submission of applications for endorsement of vegan logo and formats (March 17, 2023)
Extension of the date for the enforcement of the Food Safety and Standards (Advertising and Claims) Second Amendment Regulations, 2022 (March 17, 2023)
New FSSAI License Fee Reduction - Reduction of Initial Application Fee for New FSSAI Licenses (March 15, 2023)
Enforcement of Compliance & Standards for Non-Carbonated Water-Based Beverages (Non-Alcoholic) (March 15, 2023)
Uploading and Linking of Mandatory Lab Testing Reports - FSSAI Notification (February 15, 2023)
New Amendment Food Safety and Standards Labelling & Display Regulations (January 28, 2023)
Food Products Standards and Food Additives New Amendments in Food Safety and Standards (January 28, 2023)
Food Businesses License Renewal / Food Businesses Registrations Renewal (January 28, 2023)
FSSAI Instant Modification of License / Food License Modification (January 28, 2023)
Establishment of Pharmacovigilance System (January 11, 2023)
FSSAI caps the Penalties for Annual Returns due to Late Submission (December 27, 2022)
FSS Food Products Standards and Food Additives Amendment Regulations, 2022 (December 27, 2022)
FSSAI notifies the Second Amendment to the Food Safety and Standards (Food Products Standards and Food Additives) Regulations, 2011 (November 15, 2022)
FSSAI directs referral laboratories to analyse non-conforming parameters of the imported samples (November 15, 2022)
Approval for Non-Specified Food and Food Ingredients Regulations 2017 (November 8, 2022)
Registration of foreign food manufacturing facilities intending to export high risk food category products such as Infant food and Nutraceuticals (November 8, 2022)
FSSAI Health Certificate to import food consignment timeline extended (November 8, 2022)
FSSAI declares the restricted entry of high-risk food products in under specific ports (November 8, 2022)
FSSAI Second Amendment For Food Labelling Display Regulations (November 8, 2022)
FSSAI permits the issue of provisional NOC for imported food consignments (November 8, 2022)
Foods for Infant Nutrition Regulations, 2020 - FSSAI Food Safety Standards amendments (October 18, 2022)
FSSAI Advertising and Claims Regulations, 2018 - Food Safety Standards Amendment For Advertising and Claims (October 18, 2022)
FSSAI Prohibition and Restrictions on Sales Regulations, 2011 - FSSAI Amendment (October 18, 2022)
FSSAI notification for graphic specifications of Vegan Logo (October 13, 2022)
Draft Notification by FSSAI Labelling & Display (October 13, 2022)
FSSAI notification regarding Food Additives via First Amendment Regulations 2022 (October 13, 2022)
Health Certificate for the import of food consignments (FSSAI issues a clarification regarding the requirement) (October 13, 2022)
FSSAI clarifies uses of blends vegetable oils intended for selling as intermediary ingredients (October 13, 2022)
FSSAI update regarding the requirement of the Health Certificate (September 10, 2022)
FSSAI Advisory of AGMARK Certification for imported food products (September 10, 2022)
ePAAS - FSSAI urges Food Business Operators to submit Non-specified Food and Food Ingredients Approval (September 10, 2022)
GST collection of food businesses License/ Registration fee/ penalty (August 19, 2022)
FSSAI issues notification for the application of GST at prescribed rates on all services (August 19, 2022)
Official draft regulation on the Food Safety and Standards (Health Supplements, Nutraceuticals, Food for Special Dietary Use, Food for Special Medical Purpose, and Prebiotic and Probiotic Food) Regulations, 2022. - CliniExperts (July 27, 2022)
India presents a draft- New Drugs, Medical Devices and Cosmetics Bill, 2022 (July 21, 2022)
Prevention of Misleading Advertisements & Endorsements 2022 (July 19, 2022)
Food Safety and Standards (Food Products Standards and Food Additives) Amendment Regulations, 2022 (July 7, 2022)
Food Safety Standards (Labelling and Display) Amendment Regulations 2022 (July 7, 2022)
Central Government amendments in the Drug Rules, 1945 (July 6, 2022)
Draft of Drugs Amendment Rules, 2022 adds new drugs for OTC retail sale (July 6, 2022)
Order in continuation with the direction on FSS (Nutra) Regulations, 2022 (July 6, 2022)
Operationalization of FSS (Health supplements, Nutraceuticals, Prebiotic and Probiotic) (July 6, 2022)
Directions and procedure for regularization of the examined FDC (July 6, 2022)
Amendment in Medical Device Rules, 2017 (July 4, 2022)
Frequently Asked Questions (FAQs) on the Legal Metrology (July 4, 2022)
The Food Safety and Standards (Ayurveda Aahara) Regulations, 2022 (July 4, 2022)
Medical Device Amendment 2022 & ISO 13485 Certification Requirements (February 28, 2022)
FSS (FPS-FA) Amendment Regulations 2021 For Enzymes (February 28, 2022)
Regulation For CT Scan / MRI Equipment, All Implantable Devices (December 10, 2021)
Food Safety and Standards Regulations, 2021 (Genetically Modified or Engineered Food Organisms) (December 10, 2021)
Food Safety and Standards (FSSAI Import) First Amendment Regulations, 2021 (December 9, 2021)
The regularization of 31 FDCs has been deemed rational, and drug makers have been given six months submit applications. - CliniExperts (November 10, 2021)

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