Distance Learning

Advanced Post Graduate Diploma in Drug Regulatory Affairs ,Intellectual Property Rights and Patents

✔ 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
✔ Clinical Research Introduction | Principles of Pharmacology & Drug Discovery & Development | Roles & Responsibilities of Key Stakeholders | Preparations & Planning for Clinical Trials | Essential Documentation in Clinical Research & Regulatory Submissions | Clinical Trials Project Planning & Management | Study Start-Up Process | Clinical Monitoring Essentials | Compliance, Auditing & Quality Control in Clinical Research | Overview of Clinical Data Management and Pharmacovigilance | Introduction to Regulatory Affairs | Global Regulatory Environment | Pharma Regulations Practices & Procedures | Import and Export of Drugs in Global Pharmaceutical Industry | Common Technical Document | Good Manufacturing Practice | Quality Assurance and Regulation | Regulatory Aspects in Pharmacovigilance | Regulations Governing Clinical Trials & New Drugs | Global Drug Policy | Orphan Drugs | TRIPS and Pharma Industry | IPR Management | Patent Application