- ISO 9001 certified
- MSME · Govt of India
- Registered with MCA
Regulatory Affairs Associate Track — eCTD + Veeva Vault RIM + ANDA
Built from 437 live Regulatory Affairs Associate JDs. eCTD modules, Veeva Vault RIM, ANDA/NDA/MAA — exactly what Dr Reddy's, Sun Pharma and Aurobindo hire for.
The 30-second version
In 12 weeks you'll work on real regulatory affairs associate track — ectd + veeva vault rim + anda tasks using eCTD & FDA portals, ship End-to-end mini-ANDA package (M1 + summary M2) with… and walk out with an ISO-certified internship certificate, partner project letter and performance-based LOR. Companies hiring our learners: Dr. Reddy's, Sun Pharma, Aurobindo.
Avg salary
₹4 – 9 LPA
from real JDs
Last cohort
23/28 shipped capstone
Avg score 84/100
Top employers
Dr. Reddy's · Sun Pharma · Aurobindo · Lupin
hiring for these roles right now
Overview
What hiring managers actually ask for
Submissions and approvals across FDA, EMA and CDSCO for global health authorities.
Top JD skills
eCTD module structure (M1–M5) · ANDA / NDA / MAA basics · Labeling & artwork review · RIM tools · Variations & lifecycle
Roles you can apply for
Regulatory Affairs Associate · Publishing Specialist · Labeling Coordinator
Avg salary · Demand
₹4 – 9 LPA · High
Sample employers
Dr. Reddy's · Sun Pharma · Aurobindo · Lupin · Freyr Solutions · Indegene
Tools you'll master
Your mentor
Dr. Meera Krishnan
Lead Mentor · ex-IQVIA · 14 yrs in PV / CDM
Built PV teams at two CROs, audited by FDA twice. Trains the cohort directly through W6, then hands off to specialty mentors.
12-week syllabus
Six modules. Every module ships a deliverable.
Each module maps to a specific JD requirement so you can point recruiters to exactly which skill it proves.
Topics
- Drug approval pathways
- FDA, EMA, CDSCO, PMDA, ANVISA
- Generic vs innovator
- Lifecycle management
Deliverable·Pathway comparison brief
Satisfies JD skill
Knowledge of major regulatory frameworks
Outcomes
By the end of week 12 you can…
Concrete, role-aligned skills, not vague promises.
- Apply ectd module structure (m1–m5) to production-grade tasks
- Use eCTD + FDA portals the way Dr. Reddy's actually uses them
- Ship the capstone: End-to-end mini-ANDA package (M1 + summary M2) with publishing checklist
- Walk into interviews with a verifiable certificate, project letter & 3 work samples
- Speak the language of Regulatory Affairs Associate JDs fluently
Real projects you'll ship
Draft Module 1 (administrative) for a generic ANDA
QC review of a USPI + SmPC for label deviations
End-to-end mini-ANDA package (M1 + summary M2) with publishing checklist
Decide
You've seen what you'll ship. Lock your seat.
May 2026 cohort starts 15 May 2026. Seat fee ₹1,065. Refundable if we can't match you to a role.
Certification
Three documents, and they're verifiable
Internship Certificate
Issued by Arzon Global (ISO 9001 certified). Verifiable on /verify.
Project Certificate
Signed by the partner whose project you ship. Real signatures, real names.
Performance LOR
Awarded only if you score ≥85% across modules + capstone.
Try it
See your name on the certificate
Type your name and watch the certificate update live. The QR code links to /verify so any recruiter can confirm it's real.
Certificate ID: ARZ-REG-2026-01918
Arzon Global · Internship Certificate
ISO 9001 · MSME · MCA registered
This is to certify that
Your Name Here
has successfully completed the structured 12-week internship in
Regulatory Affairs Associate Track — eCTD + Veeva Vault RIM + ANDA
Certificate ID
ARZ-REG-2026-01918
Verified Regulatory Affairs Internship Certificate + Project Letter.
FAQs
Quick answers to the usual questions
Is this Regulatory Affairs Associate Track — eCTD + Veeva Vault RIM + ANDA programme suitable for freshers?+
Yes. The first two weeks are foundational, we don't assume prior pharmacy & life sciences experience. By W4 you'll be working on real data.
Do I get a job guarantee?+
No. Anyone promising guaranteed jobs is breaking ASCI guidelines. We guarantee live mentoring, real-data work, a verifiable certificate, and structured interview access with our hiring partners. See /proof for our refund policy.
How are sessions delivered?+
Live cohort calls 3 evenings a week (90 min each), recordings within 12 hours, async Slack with mentor SLA of 1 hour during cohort hours. The browser-based player tracks your progress.
What if I miss a live session?+
Recordings are available the same day. You can mark lessons complete in the player and submit assignments asynchronously. Mentors do weekend office hours for catch-up.
What does the certificate actually say?+
It states you completed the structured 12-week internship in Regulatory Affairs Associate Track — eCTD + Veeva Vault RIM + ANDA, all six modules, the capstone, and met our performance bar. It carries a unique ID + QR code that resolves on /verify. Try the sample on the certificate page.
Can I pay in instalments?+
Yes, 0% EMI through Razorpay (3 / 6 / 9 months). A ₹1,065 refundable deposit locks your seat; the balance is due 3 days before the cohort starts.
Ready when you are
Join the May 2026 cohort of Regulatory Affairs Associate Track — eCTD + Veeva Vault RIM + ANDA
Starts 15 May 2026. Seat fee ₹1,065. Walk out with an ISO-certified internship certificate and a recruiter-ready portfolio.