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Clarification on Labeling Permissions under Rule 104A of Drugs and Cosmetics Rules, 1945

Posted by: admin May 31, 2025

Guidelines on Disposal of Expired/Unused Drugs

Posted by: admin May 31, 2025

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31st May, 2025

Guidelines for acceptance of recycled Polyethylene terephthalate (PET) as Food Contact Material (FCM-rPET)

Posted by: admin May 31, 2025

Discontinuation of the Term “100%” on Food Product Labels and Related Promotional Materials- reg.

Posted by: admin May 31, 2025

Unapproved/Approved New Drugs Manufacturing NoC for Export Purposes

Posted by: admin May 20, 2025

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20th May, 2025

Long awaited revamp of Revised Guidelines on Similar Biologics- Regulatory requirements for Marketing Authorization

Posted by: Hitesh Gupta May 16, 2025

Public Notice on Regulation of Export of Codeine Phosphate Preparations

Posted by: Hitesh Gupta May 16, 2025

7
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16th May, 2025

Refined Zinc (Quality Control) Order, 2025

Posted by: Hitesh Gupta May 7, 2025

7
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7th May, 2025

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Regulation/Guidelines

Organic Food Labelling In India| Certification, and Import of Organic Food in India

This Article is All About Organic Food Labelling In India and Certification, and Import of Organic Food in India. Explained in Detail About What is Organic Food labelling? Summary Organic...

21st April, 2025

Regulation/Guidelines

Cosmetic Label Compliance India : A Guide to Compliance

Introduction Looking for Cosmetic Label Compliance India? Are you a cosmetic manufacturer or importer navigating the complex world of Indian regulations? Ensuring your product labels comply with the latest cosmetic...

26th March, 2025

Regulation/Guidelines

Clinical Investigation Approvals: An Overview of Forms MD-22 and MD-23

Summary As per MDR 2017, “clinical investigation” means the systematic study of an investigational medical device in or on human participants to assess its safety, performance or effectiveness. Clinical investigations...

15th January, 2025

Regulation/Guidelines

Regulatory Challenges of SaMD: Navigating Global Standards and Compliance

Overview Navigating Software as a Medical Device regulation involves addressing varying global standards, including risk-based classifications. Challenges include managing risks, demonstrating clinical evidence, and ensuring data security. Harmonisation efforts and...

4th November, 2024

Manufacturer

Manufacturer

Clarification on Labeling Permissions under Rule 104A of Drugs and Cosmetics Rules, 1945

Guidelines on Disposal of Expired/Unused Drugs

Guidelines for acceptance of recycled Polyethylene terephthalate (PET) as Food Contact Material (FCM-rPET)

Discontinuation of the Term “100%” on Food Product Labels and Related Promotional Materials- reg.

Unapproved/Approved New Drugs Manufacturing NoC for Export Purposes

Long awaited revamp of Revised Guidelines on Similar Biologics- Regulatory requirements for Marketing Authorization

Public Notice on Regulation of Export of Codeine Phosphate Preparations

Refined Zinc (Quality Control) Order, 2025

For Importers To India

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For Manufacturer in India

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