Global Regulatory Affairs Program
Pharma Regulatory Affairs • Medical Devices • US FDA • EU MDR • CDSCO
Build a high-growth career in Regulatory Affairs with comprehensive, industry-focused training covering global regulatory frameworks, dossier preparation, and submission pathways across major markets.
Program Snapshot
Duration: 3 Months
Training Mode: Online + Internship
Certification: Industry-Recognized Certificate
Who Can Apply: Life Sciences, Pharmacy, Biotechnology & Related Graduates
Coverage: Pharma Regulatory Affairs + Medical Devices
Markets: US FDA, EU MDR/EMA, CDSCO (India), Global ROW
Program Overview
This program provides comprehensive, industry-focused training in global regulatory affairs for pharmaceuticals and medical devices. It covers regulatory frameworks, submission pathways, and compliance requirements across major markets including US FDA, EU MDR/EMA, and CDSCO (India).
Designed with a practical approach, this program equips participants with hands-on experience in dossier preparation, regulatory submissions, and post-market compliance — preparing them for real industry roles from day one.
Who Should Enroll
This program is ideal for:
Life Sciences, Pharmacy, Biotechnology & Related Graduates
Fresh graduates seeking careers in pharma and medical devices regulatory roles
Working professionals looking to transition into regulatory affairs
Individuals aiming to work with US FDA, EU MDR, or CDSCO submissions
Pharma / biotech professionals who want to upskill in global compliance
Program Highlights
Coverage of US FDA, EU MDR/EMA, CDSCO & global frameworks
Dual focus: Pharma Regulatory Affairs + Medical Devices RA
Hands-on dossier preparation (CTD, ACTD, Technical File)
ISO 14971 risk management & IEC 62366 usability engineering
Real-time case studies and submission process walkthroughs
Career guidance, resume building & interview preparation
What You Will Learn
Career Opportunities After Completion
Graduates of this program can pursue roles such as:
Regulatory Affairs Associate
Regulatory Affairs Specialist (Medical Devices)
Regulatory Documentation Specialist
Submission Analyst
Clinical Evaluation Specialist
PMS / Vigilance Specialist
Quality & Regulatory Associate (ISO 13485)
Program Outcome
Become industry-ready with strong expertise in global regulatory submissions for pharmaceuticals and medical devices, including hands-on exposure to EU MDR, US FDA, and CDSCO requirements — positioned to enter regulatory affairs roles from day one.
Placement Support
We provide structured career support to help you transition into industry roles:
Dedicated placement assistance
Technical & HR interview preparation
Resume writing and LinkedIn profile optimization
Ongoing job support with pharma companies, CROs, and medical device firms
How to Enroll
Submit the online enrollment form
Attend a free career counseling session
Complete fee payment & confirm your batch
Begin training with onboarding & LMS access
Start Your Career in Global Regulatory Affairs
Take the next step toward a rewarding regulatory career with Verivance Academy's Global Regulatory Affairs Program — covering pharma, medical devices, and global compliance.