Regulatory Affairs Internship
Regulatory Affairs Internship (DRA)
A Drug Regulatory Affairs (DRA) internship that prepares you for one of the highest-paying pharma career tracks — CDSCO, US-FDA, EMA, eCTD, ANDA and DMF submissions, taught by working RA leads.
1 Month2 Months3 Months4 Months6 Months
Who it's for
Eligibility
- B.Pharm
- M.Pharm (Pharmaceutical Regulatory Affairs)
- M.Sc Biotechnology
- Pharm.D
Curriculum
What you'll learn
01Indian regulations (CDSCO, DCG(I))
02US-FDA & ANDA
03EU MAA & eCTD
04DMF preparation
05Labelling & artwork compliance
Where it's used
Industry applications
Pharma regulatory submissions Biosimilar regulatory Medical device regulatory Nutraceutical regulatory Cosmetic regulatory
Career outcomes
Roles you can target
- Regulatory Affairs Associate
- DRA Executive
- Regulatory Publishing Specialist
- Medical Writer
- Labelling Specialist
BioBridge Verified Internship Certificate
On completion you receive a verifiable digital certificate with a unique ID. Recruiters can validate authenticity at biobridgeind.com/verify — no PDFs to forge.
See sample verificationFAQ
Common questions
Is the curriculum aligned with M.Pharm DRA?
Yes — it complements the PCI M.Pharm Pharmaceutical Regulatory Affairs syllabus with live industry case studies.
Start your regulatory affairs internship today
Register free, pick your duration, and start in the next cohort.