ICH GCP Clinical Research - R3 ; ICMR Guidelines & NDCT Rules 2010

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ICH GCP Clinical Research - R3 ; ICMR Guidelines & NDCT Rules 2010
pharmaceutical business analytics distance course
Distance Learning
  • ✔ CPD Accredited - Continuing Professional Development
  • ✔ Program developed by senior industry experts
  • ✔ eBooks – Presentation & Notes on Cliniminds LMS
  • ✔ Cliniminds Certification after completion of program
  • ✔ MCQ based final exams
  • ✔ GCP—Background, Development & Implementation | Purpose & Principles of ICH-GCP | Overview of Changes: E6 R(2) & R(3) | Institutional Review Board/Independent Ethics Committee (IRB/IEC) | Stakeholders | Sponsor/Investigator Responsibilities | Clinical Trial Protocol & Protocol Amendments | Investigator’s Brochure | Essential Documents for the Conduct of a Clinical Trial | Introduction to E3 Addendum

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ICH GCP Clinical Research - R3 ; ICMR Guidelines & NDCT Rules 2010 Course Details

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