ADRMS User Manual for Stakeholders on Medical Device Adverse Event Reporting

Posted by: Prabhas Chakraborty August 31, 2026

7
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31st August, 2026

NCC-MvPI Issues ADRMS User Manual for Medical Device Adverse Event Reporting

Posted by: Hitesh Gupta August 31, 2026

7
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31st August, 2026

CDSCO Reports Risk-Based Inspections of Pharmaceutical Manufacturing Units

Posted by: Prabhas Chakraborty August 31, 2026

7
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31st August, 2026

Medical Devices (Second Amendment) Rules, 2026: New Sterilization Labelling Requirements and Testing Fees

Posted by: Hitesh Gupta August 31, 2026

Restriction on all formulations of FDCs containing Chlorpheniramine Maleate and Phenylephrine Hydrochloride with mandatory warning against use in children below four years of age

Posted by: Hitesh Gupta August 26, 2026

Establishment of a TGSAFE (Telangana Standards Authority for Food and Essential drugs) through merger of the Food Safety and the Drugs Control Department under Health, Medical & Family Welfare (G) Department (HM&FW)

Posted by: Hitesh Gupta August 25, 2026

ICMR and CDSCO Invite Stakeholder Comments on Standard IVD Performance Evaluation Protocols for Scrub Typhus

Posted by: Prabhas Chakraborty August 24, 2026

FSSAI Notifies Packaging Amendment Regulations, 2026 for Pan Masala Packaging

Posted by: Prabhas Chakraborty August 24, 2026

7
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24th August, 2026

What's New 2?

Regulation/Guidelines

The Cosmeceuticals Grey Zone: When a Cosmetic Claim Risks Becoming a Drug Claim

“Cosmeceutical” is a popular marketing word. It suggests something more powerful than an ordinary Cosmetic — a product that treats skin condition, not just improves appearance. The problem is that...

7th September, 2026

Regulation/Guidelines

Ingredient Safety Dossiers: Building a Defensible Package for Novel Actives

Companies developing Cosmetics with new or unusual active ingredients face a higher regulatory bar in India than those using well-established formulations. Understanding what “new” means under the Cosmetics Rules, 2020,...

2nd September, 2026

Regulation/Guidelines

Cosmetic Claims Substantiation: What Counts as Evidence Under Indian Rules

Walk down any Cosmetics aisle and you will see claims like “clinically proven,” “dermatologist tested,” or “reduces fine lines in two weeks.” These claims sell products — but under the...

26th August, 2026

Regulation/Guidelines

AI/ML-Based Medical Devices — Emerging Regulatory Questions

Traditional Medical Device regulation assumes a fixed product: what’s approved is what ships, indefinitely, until a formal change is filed and reviewed. Adaptive AI and machine learning algorithms break that...

24th August, 2026

ADRMS User Manual for Stakeholders on Medical Device Adverse Event Reporting

NCC-MvPI Issues ADRMS User Manual for Medical Device Adverse Event Reporting

CDSCO Reports Risk-Based Inspections of Pharmaceutical Manufacturing Units

Medical Devices (Second Amendment) Rules, 2026: New Sterilization Labelling Requirements and Testing Fees

Restriction on all formulations of FDCs containing Chlorpheniramine Maleate and Phenylephrine Hydrochloride with mandatory warning against use in children below four years of age

Establishment of a TGSAFE (Telangana Standards Authority for Food and Essential drugs) through merger of the Food Safety and the Drugs Control Department under Health, Medical & Family Welfare (G) Department (HM&FW)

ICMR and CDSCO Invite Stakeholder Comments on Standard IVD Performance Evaluation Protocols for Scrub Typhus

FSSAI Notifies Packaging Amendment Regulations, 2026 for Pan Masala Packaging

For Importers To India

Drug

Biologicals

Food Supplements

Medical Device

IVD

Food

Cosmetic

Other

For Manufacturer in India

Drug

Biologicals

Food Supplements

Food

Medical Device

IVD

Cosmetic

Other