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  1 - Introduction

   1 - What is ICH English.vtt

   2 - ICHGCPHistory.pdf

   2 - The Declaration of Helsinki.mp4

   3 - The future of ICH English.vtt

  2 - Definitions of terms

   4 - GCP and Clinical Study English.vtt

   5 - Key stakeholders in a Clinical Study English.vtt

   6 - Key Processes in a Clinical Study English.vtt

   7 - Examplesofsourcedocuments.pdf

   7 - Key Essential Documents.mp4

   8 - Investigational Products IPs.mp4

  3 - The 13 Principles of ICHGCP R2

   9 - Principles of GCP.mp4

  4 - Responsibilities of the Investigator

   10 - Qualifications and Agreements.mp4

   11 - Adequate Resources ADDENDUM R2.mp4

   12 - Medical Care of Trial Subjects.mp4

   13 - Communication with IRB IEC.mp4

   14 - Compliance with Protocol.mp4

   15 - IPs Randomization Procedures and Unblinding.mp4

   16 - Informed Consent of Trial Subjects.mp4

   17 - Records and Reports ADDENDUM R2 English.vtt

   18 - Progress Report and Safety Reporting English.vtt

   19 - Premature Termination or Suspension of a Trial and Final Report by Investigator English.vtt

   3 - Investigators responsibilities.html