Indian Pharmacopoeia Commission

Indian Pharmacopoeia Commission Issues Public Notice on National Formulary of India (NFI) 2026

Posted by: Prabhas Chakraborty October 29, 2026

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29th October, 2026

ADRMS User Manual for Stakeholders on Medical Device Adverse Event Reporting

Posted by: Prabhas Chakraborty August 31, 2026

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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

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31st August, 2026

Indian Pharmacopoeia 2026- Amendment Lists

Posted by: Hitesh Gupta June 29, 2026

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29th June, 2026

Strengthening Adverse Event Reporting under the Materiovigilance Programme of India (MvPI) – Compliance by Medical Device Marketing Authorisation Holders

Posted by: Prabhas Chakraborty February 17, 2026

What's New 2?

Regulation/Guidelines

Schedule M Revisions: How Will They Impact Pharmaceutical Manufacturers?

What a Revised Schedule M raises GMP standards in India, what has changed for manufacturers, and how large firms and MSMEs can prepare for Compliance and CDSCO inspections. Revised Schedule...

12th November, 2026

Regulation/Guidelines

CDSCO vs US FDA vs EMA: Why the Same Drug Faces Different Approval Requirements

A practical comparison of CDSCO vs FDA vs EMA, explaining how each regulator's Drug approval process differs and why one Drug needs separate approvals in India, the US and Europe....

2nd November, 2026

Regulation/Guidelines

How to Manufacture Class A & B Medical Devices in India: State FDA License Guide

A quick guide on the Class A & B Medical Device manufacturing license — covering State FDA rules, Form MD-3/MD-5, fees, and timelines for manufacturers. Every manufacturer entering India's device...

21st September, 2026

Regulation/Guidelines

Importing Small Quantities of Cosmetics for R&D in India: NOC Requirements

A brief guide on Cosmetic import NOC India — covering when small quantity Cosmetic import for R&D testing bypasses full registration under Cosmetic rules 2020. Not every Cosmetic shipment into...