Home - Prequalification: Training material for seminars and workshops
| Training material |
| The following is a collection of WHO/QSM training packages and various resources from workshops and seminars. |
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Meetings Meeting with Stakeholders and Manufacturers
WHO Medicines Prequalification in a New Decade
5th Consultative Stakeholder Meeting for UN Prequalification of Diagnostics, Medicines and Vaccines
4th Consultative Stakeholder Meeting for UN Prequalification of Diagnostics, Medicines and Vaccines
3rd Consultative Stakeholder Meeting for UN Prequalification of Diagnostics, Medicines and Vaccines
2nd Consultative Stakeholder Meeting for UN Prequalification of Diagnostics and Medicines
1st Consultative Stakeholder Meeting for UN Prequalification of Diagnostics and Medicines
Training Workshop on Pharmaceutical Development with a Focus on Paediatric Formulations
Training Workshop on selected GMP topics for pharmaceutical manufacturers and GMP inspectors
Training Workshop on Quality Documentation of Generic medicines in CTD Format
Third Annual Prequalification Assessment Training
Training Workshop on WHO Prequalification of Medicines Programme
Workshop on assessment of bioequivalence data submitted to regulatory authorities
Training Workshop on Pharmaceutical Development with a Focus on Paediatric Formulations
Conference on Quality of Active Pharmaceutical Ingredients
Planning, conduct and regulatory assessment of stability studies
WHO Seminar for European Manufacturers and EU Holders of Marketing Authorizations
Manufacture of sterile medicines - advanced training workshop for State Food and Drug Administration (SFDA) GMP inspectors
WHO workshop on assessment of bioequivalence data submitted to regulatory authorities
Advanced Training Workshop on WHO prequalification requirements for Reproductive Health and Seminar for Indonesian Manufacturers on WHO Prequalification Programme
Interregional Seminar for Quality Control Laboratories involved in WHO Prequalification Programme and/or participating in respective sampling and testing projects
Training Workshop on Assessment of Interchangeable Multisource Medicines
Training Workshop on Regulatory Requirements for Registration of Artemisinin Based Combined Medicines and Assessment of Data Submitted to Regulatory Authorities
WHO/FIP Training Workshop on Pharmaceutical Development with a Focus on Paediatric Formulations
Training Seminar for Quality Control Laboratories on Quality Assurance, Prequalification and Development of Standards
Training Seminar for Quality Control Laboratories on Quality Assurance, Prequalification and Quality Control
Pharmaceutical Quality, Good Manufacturing Practice and Bioequivalence with a Focus on TB products
Training Workshop on Pharmaceutical Development with a Focus on Paediatric Formulations
EAC/TFDA/WHO training for East Africa Community National Medicine Regulatory Authorities staff on assessment of dossiers based on WHO Prequalification guidelines.
WHO/FIP Training Workshop on Dissolution, Pharmaceutical Product Interchangeability and Biopharmaceuticals Classification System (BCS)
WHO Prequalification Programme Meeting on Priority Essential Medicines
WHO/FIP Training Workshop on Pharmaceutical Development with a Focus on Paediatric Medicines
Training Workshop on Pharmaceutical Quality, Good Manufacturing Practice and Bioequivalence with a Focus on Artemisinines
GCP Seminar for Inspectors Participating in the WHO Prequalification Programme
Training Workshop on Pharmaceutical Quality and Bioequivalence
Pharmaceutical Quality, Good Manufacturing Practice and Bioequivalence with a Focus on Artemisinines
Pharmaceutical Quality, Good Manufacturing Practice and Bioequivalence
Good Manufacturing Practices (GMP) by the World Health Organization (WHO), to inspectors from the State Drug Administration (SFDA)
Good Manufacturing Practices (GMP) by the World Health Organization (WHO); training for inspectors from the Medicines Regulatory Authority
GMP and Quality Assurance of HIV products including Bioequivalence issues
GMP and Quality Assurance of TB products including Bioequivalence issues
GMP and Quality assurance of antimalarial medicines with emphasis on Prequalification of Artemisinin-based combination products (ACTs)
Pharmacovigilance: First Training workshop to introduce monitoring of safety and efficacy of antiretrovirals in Africa
Prequalification of Antimalarial Drug Products, World Health Organization
Prequalification of finished pharmaceutical products (FPPs) used in the treatment of HIV/AIDS, Malaria and Tuberculosis
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Good manufacturing Practices (GMP) Training modules