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

Cliniminds Corporate Presentation

Drug Regulatory Affairs ,Intellectual Property Rights and Patents

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
✔ 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

Download Full Brochure

Drug Regulatory Affairs ,Intellectual Property Rights and Patents Course Details

Whatsapp Linkedin Youtube Instagram Facebook Blogspot