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Drug | Cosmetic

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 M is the b..

12th November, 2026

Drug

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. A Drug approve..

2nd November, 2026

Medical Device

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..

21st September, 2026