Instructor-led courses
30 April 2025
| Meeting report

Overview
Health Products Regulation and Prequalification Learning Catalogue
Below you will find instructor-led courses.
- WHO Good Regulatory Practices
- Assessors Training: The WHO Global Benchmarking Tool to Benchmark Regulatory Authorities
- Quality management system implementation workshop
- Regulatory performance indicators
- WHO-Swissmedic Regulatory Peer Training
- Regulatory Preparedness for Provision of Marketing Authorization of Vaccines in Public Health Emergencies
- Assessment of bioequivalence studies
- Basic Training on the Assessment of Dossier in the Common Technical Document Format
- Substandard and Falsified Medical Products: Prevention, Detection, Response
- Post-market and Market Surveillance of In Vitro Diagnostics for Testing Providers and Regulators
- Principles of Scientific Assessment of an In Vitro Diagnostic Dossier: Demonstration of Quality, Safety and Performance and the Procedural/Administrative Aspects of Technical Files Assessment and Marketing Authorization within the National Regulatory Authorities
- GMP inspection: basic course
- GMP inspection: advanced course
- GMP: deficiencies classification
- Good Storage and Distribution Practices Regulatory Inspections Using a Risk-Based Approach
- National AEFI data management training using Vigitools
- Vaccine safety basics course
- Vaccine safety communication course
- National AEFI guidelines dissemination course
- Intermediate course on AEFI
- AEFI signal detection course
- Advanced course on AEFI and causality assessment
- AEFI field investigation and communication simulation course
- AEFI causality assessment for AEFI review committee members
- Prequalification of Medicines Annual Training for Regulators: Quality Assessment
- Prequalification of Medicines Annual Training for Regulators: Biotherapeutic Product and Similar Biotherapeutic Product Assessment
WHO Team
Regulation and Prequalification (RPQ)