Advanced Post Graduate Diploma in Drug Regulatory Affairs

Cliniminds Corporate Presentation

Drug Regulatory Affairs

pharmaceutical business analytics distance course

Distance Learning

✔ ACCRE USA Accredited
✔ Program developed by senior industry experts
✔ eBooks – Presentation & Notes on Cliniminds LMS
✔ Cliniminds Certification after completion of program
✔ MCQ based final exams
✔ Introduction to Regulatory Affairs | Pharma Regulations Practices and Procedure | Global Pharmaceutical Industry Scenario | Indian Pharmaceutical Industry | Global Regulatory Environment | Regulations Governing Clinical Trials and New Drugs Schedule Y | Regulatory Inspections in Clinical Research (FDA, EMEA, UK, and Indian) | Future of Regulatory Compliance | Orphan Drugs | Import and Export of Drugs | Good Manufacturing Practice | Quality Assurance and Regulations | Global Drug Policies | Regulation in Pharmaceutical Devices | TRIPPs and Pharma Industry | Intellectual Property Right Management | Patents | Pharmacovigilance (Introduction, global reporting requirements)

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Drug Regulatory Affairs Course Details

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