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

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Drug Regulatory Affairs ,Intellectual Property Rights and Patents

Live eLearning - Fulltime & Weekend

✔ ACCRE USA Accredited
✔ Assured Placement Support – 9500+ Placements
✔ Hands on Training on Industry Softwares
✔ Senior industry experienced faculty
✔ Built-in Internship with CRO & life sciences firm
✔ Live eLearning Session
✔ Cliniminds LMS - eBooks & Audio Video Recordings of Live Sessions
✔ 3 Certifications after successful completion of program

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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

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Cliniminds Corporate Presentation

Drug Regulatory Affairs ,Intellectual Property Rights and Patents Course Details

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