Certification program
3 Month Certification Course in Drug Regulatory Affairs
Regulatory submissions · Global compliance · Lifecycle management
Online (live + recordings)
Weekends
40 seats
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Talk to our counselors for batch schedule and enrollment. Fees shared on enquiry.
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About this course
3 Month Certification Course in Drug Regulatory Affairs from Global Pharma Academy (MSME & ISO 9001:2015). Focus on regulatory submissions, global compliance, safety & efficacy, and lifecycle management.
Why choose this course
Certificate Provided
Study Material Provided
Recording provided
100% placement assistance
Learn from top industry Experts
Syllabus
1
Regulatory Submissions
2
Global Compliance
3
Safety & Efficacy
4
Lifecycle Management
5
CTD / eCTD
6
India / US / EU regulations
Skill development
Resume preparation
HR interview questions
Job searching skills
English communication skills
Basic technical skills
Aptitude test
Mock interview
Group discussion
Presentation skills
How to enroll
1
Pay via Razorpay OR GPay/PhonePe/Paytm to 9423272876.
2
Share screenshot on WhatsApp to 9423272876.
3
Confirmation email; WhatsApp group 1 day before Class 1.
4
Admissions open till 40 seats fill. Queries: globalpharmaacademy@gmail.com
FAQ
Course completion certificate from Global Pharma Academy (ISO & MSME certified).
Yes, two installments.
Drug regulatory affairs specialist / associate / trainee.
CROs, healthcare IT, corporate offices of manufacturing companies.
Average ₹1.8–3.6 LPA.
Possible after couple of years per organization policy.
Pharmacy, life sciences, medical science.
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