Advanced Post Graduate Diploma in Drug Regulatory Affairs & Pharmacovigilance

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Advanced Post Graduate Diploma in Drug Regulatory Affairs & Pharmacovigilance
e-learning
Live eLearning - Weekend
  • ✔ ACCRE USA Accredited
  • ✔ Assured Placement Support – 11500+ 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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Advanced Post Graduate Diploma in Drug Regulatory Affairs & Pharmacovigilance
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) | Overview of Clinical Research | Pharmacology- General Principles | Introduction, Definition & Methods in Pharmacovigilance | Essentials Documents in Pharmacovigilance | Pharmacovigilance Regulations | Safety Reporting (including Medical Information) and Processing ICSR | Aggregate reports, Signal detection & Risk Management | Audits and Inspections | Advanced Pharmacovigilance & Analytics | Hands On Training on Case Processing and Report generation

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Drug Regulatory Affairs & Pharmacovigilance Course Details

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