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Pharm (Regulatory Affairs) Course is a specialized branch that focuses on ensuring that drugs, biologics, and medical devices are developed, manufactured, tested, and marketed in compliance with the regulatory requirements of national and international health authorities.
Duration
2 Years (Four Semesters)
course fee
| Fee Per Semester |
Fee Per Year |
|
| FOR BHUBANESWAR CAMPUS | Rs 1,70,000 |
Scope/Job Opportunity
Pharmaceutical Regulatory Affairs offers one of the most stable and rewarding career paths in the pharmaceutical, biotechnology, and medical device sectors. Regulatory Affairs (RA) professionals can work in different roles depending on their experience and qualifications. RA is an internationally recognized profession. Professionals with knowledge of ICH guidelines, USFDA, EMA, CDSCO (India) have excellent job opportunities in following areas.
- Regulatory Affairs Associate
- Regulatory Affairs Coordinator
- Regulatory Executive
- Regulatory Affairs Specialist
- Regulatory Affairs Officer
- Regulatory Affairs Manager
- Director of Regulatory Affairs
- Head of Regulatory Strategy
- Regulatory Labelling Specialist
- Regulatory Intelligence Analyst
- Pharmacovigilance & Safety Specialist
Career Path
- Pharmacovigilance & Drug Safety
- Quality Assurance / Quality Control
- Clinical Research & Development
- Regulatory Consulting
- Regulatory Policy / Government Agencies (CDSCO, USFDA, EMA, WHO, etc.)