Post Graduate Diploma in Drug Regulatory Affairs - Part Time
Post Graduate Diploma
In Pune
Description
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Type
Post Graduate Diploma
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Location
Pune
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Duration
6 Months
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Start date
Different dates available
To create a thorough understanding of important regulatory concepts
To create experts in the field of RA documentation and research.
To encourage continuous learning and development of RA field.
Course StructureToptop
The Aims & Structure of Regulation
Regulatory Strategy
Marketing Authorization
Non – Clinical Studies
Clinical Trials
Submission & Review
Good Manufacturing Practice (GMP)
Facilities
Location
Start date
Start date
About this course
To Develop Knowledge and Skills for Regulatory Affairs
Graduates in any stream of science are eligible to apply.
Final Year Students can also apply.
Reviews
Subjects
- Regulation
- Clinical Studies
- World Affairs
- Regulatory Strategy
- Good Manufacturing Practice (GMP)
- Marketing Authorization
- Drug Laws
- Marketing
- Research
- Pharmacodynamics
Teachers and trainers (1)
Global Institute of Regulatory Affairs
Drug Regulatory Affairs
Course programme
- The Aims & Structure of Regulation
- Regulatory Strategy
- Marketing Authorization
- Non – Clinical Studies
- Clinical Trials
- Submission & Review
- Good Manufacturing Practice (GMP)
- Type of companies hiring RA professionals
- Pharmaceutical
- Medical Devices
- In Vitro Diagnostics
- Biologics and Biotechnology
- Veterinary Products
- Cosmetics
- Local FDA/ US FDA/UK MHRA/EDQM
- Ministry of Health/DCGI
- Clinical Research Organization/ Contract Research Organization
- Pharmaceutical consultancy companies
- RA professional can get employment as
- Regulatory Affairs Associates
- Regulatory Affairs Assistance
- Regulatory Affairs head/ Director
- Medical Information Associates
- Drug Inspector/Drug Controller/
- Drug Safety Specialist/ Regulatory Food Safety Scientist
- Quality Operations/Quality Control/Quality Assurance
- Regulatory Affairs Consultants
Post Graduate Diploma in Drug Regulatory Affairs - Part Time