Hello everyone!
If you’re looking for a non-lab, documentation-heavy, yet impactful role in the pharma industry — Regulatory Affairs might be your calling.
What is Regulatory Affairs?
RA professionals ensure that pharmaceutical products meet required legal and scientific standards before being approved for sale or use.
A. Core Responsibilities:
•Preparing dossiers for DCGI, USFDA, EMA, etc.
•Responding to regulatory queries.
•Managing product registration for domestic and international markets.
•Ensuring label/package compliance with rules.
B. How to Enter RA?
•B.Pharm or M.Pharm (Quality Assurance/Pharmaceutics/Regulatory).
•PG Diploma or certification in Regulatory Affairs (optional but helpful).
•Strong communication and documentation skills required.