Intermediate

ICH E6 – Investigator (Chapter 4) (R2)

Hazardous Waste Generator

WHO Guidance on Good Clinical Laboratory Practices

ICH Q9 – Quality Risk Management

Human Error Prevention

Good Distribution Practices: Operational Principles

Technical Writing in a Regulated or Accredited Environment

EU Medical Device Regulation (EU MDR) – Chapter 9 – Confidentiality, Data Protection, Funding and Penalties

EU Medical Device Regulation (EU MDR) – Chapter 7 – Post Market Surveillance, Vigilance and Market Surveillance

EU Medical Device Regulation (EU MDR) – Chapter 10 – Final Provisions