Good Clinical Practice (GCP) — ICH E6(R3)

Investigator Site Personnel Training

The ethical and regulatory foundation every person working on a clinical trial site is expected to know: where GCP came from, what ICH E6(R3) requires, and how to apply it under pressure.

30 lessons, about 206 minutes. Free, in your language.

Introduction to Clinical Research and GCP

Roles and Responsibilities in Clinical Trials

Clinical Trial Protocol and Design

Informed Consent Process

Risk Management and Quality by Design

Investigational Product (IP) Management

Data Collection, Source Documentation and CRFs

Safety Reporting and Pharmacovigilance

Audits, Inspections and Compliance

Clinical Trial Closure and Archiving