Good Clinical Practices (GCP)

Good Documentation Practices – Time Format

Good Documentation Practices – Date Format

Why Good Documentation Practices are Critical in a GMP Environment

The Fundamentals of Corrective and Preventive Actions (CAPA)

ICH E6 – Clinical Trial Protocol and Protocol Amendments (Chapter 6) (R2)

Technical Writing in a Regulated or Accredited Environment

Inspection Readiness: Your Role & Preparing for Inspector Interactions

ICH E6 – Institutional Review Board / Independent Ethics Committee (IRB/IEC) (Chapter 3) R2

ICH E6 – Introduction and Principles of Good Clinical Practices (GCP) (Sections 1-2) R2

The General Rules of Good Documentation Practices & Data Integrity