Announcing ‘3 months certification course in drug regulatory affairs ‘ batch 12

Happy to announce 3 months online certification course in Drug Regulatory affairs batch 12

Fill this Google form to know more about the course
https://docs.google.com/forms/d/e/1FA...

Syllabus
Topics covered
Class 1
i)Introduction
ii)Definition, Rationale, iii)Roles and responsibilities
Class 2
i)How Regulatory Affairs works in Pharmaceutical Company
ii)Different Regulatory Authorities
iii)Innovator and Generic Drugs
iv) Drug development process
Class 3
i)Different guidelines used in Regulatory work.
Class 4
i) ICH Guidelines
In depth Quality guidelines and Overview of Safety, Efficacy and Multidisciplinary guidelines
Class 5
CTD Structure
In depth Module wise content detailing
Class 6
i)ACTD Structure
In depth Part wise content detailing
ii) Difference between CTD and ACTD
Class 7
Dossier filing process for Europe, USA and Rest of world market
Class 8
Different types of documents required for Dossier preparation and their explanation
Class 9
Post approval process: Variations and Renewals
class 10
Overview of medical device regulatory
Class 11
Overview of Clinical Trials and their phases, Pharmacovigilance, PSUR
Class 12
Frequently asked interview questions with answers

Timing for class
1 pm to 3pm (2 hours weekly on Saturday and Sunday)
All classes are virtual through Zoho
Course will starts from 28 september 2025 onwards

Benefits
1) certificate from ISO certified organization
2) expert learning
3)Recorded lectures
4)domain knowledge
5)Placement assistance
6)Soft skill development

Who can ENROLL
Anyone who wish to learn Drug Regulatory Affairs from science background

One time fees :- (7999/-)
Click here to pay :-
https://rzp.io/rzp/MvX1ehuX

2 installment fees :- ( 8999/- Second installment need to pay in 21 days)
Click here to pay:- https://rzp.io/rzp/UXbqEsW9
Or
How to enrol
Pay online via gpay/phonepay/paytm to 9423272876

After payment share screenshot to 9423272876 via whatsup

After payment from any above mentioned way you will get confirmation email.
You will be added to Whatsup group one day prior to Class 1
All admissions opens till seats fulfilment (40)
If any query email us at [email protected]

Frequently asked questions
1) Which certification we get after this course
Answer- You will get certification of course completion from Global Pharma Academy which is ISO and MSME certified
2) Details about Global Pharma Academy
Answer- Visit at www.globalpharmaacademy.com
3) can we pay fees in installment
Answer- Yes you can pay fees in two installments
4) Is this course is for freshers or experience people
Answer- This course is ideally created for freshers and early level experience student
5) Can i get help for placement after this course
Answer- We will help to prepare for interview and also work on soft skills so that you can give your best during actual interview
6) How many seats are there
Answer- 40
7) Can i get recording of class
Answer- Yes, you can get live class and recording as well
8) can I access this class from mobile also?
Answer-Yes you can
9) which job i can get after this course
Answer- You can get opportunities as drug regulatory affairs specialist/associate/trainee
10) In which companies i can get job after this course
Answer- In CRO (Contract research organizations), healthcare IT, corporate offices of manufacturing companies
11) In which location i can get job after this course
Answer- We can provide opportunities all over india, mostly jobs available in metro cities and industrial area
12) How much package i can get after this course in job
Answer- Package will be differ from company to company but average anyone can get 1.8-3.6 LPA in between


we are also available on mobile application..download from following links to get in touch with us
Here are links android link https://play.google.com/store/apps/de...

IOS link https://apps.apple.com/in/app/classpl...
Web link Web.classplusapp.com Org code - unhsuc