Regulatory Affairs (RA) professionals ensure that medicines meet all legal and scientific requirements before hitting the market.
Responsibilities:
1.Prepare and submit drug approval documents (like dossiers)
2.Communicate with agencies like DCGI, USFDA, EMA
3.Ensure labeling, packaging, and manufacturing follow guidelines
• Entry after B.Pharm/M.Pharm (preferably in QA or Pharmaceutics)
• RA roles are in high demand due to frequent drug launches and global expansion.
Interested in RA? Share your questions or experiences below!
