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Agenda XI CPANDRH
Agenda XI CPARF
Meeting Documents
Market research to identify and analyze opportunities to produce strategic health technologies in Latin America and the Caribbean
Market research to identify and analyze opportunities to produce strategic health technologies in Latin America and the Caribbean
Technical and scientific products
WHO Expert Committee on Specifications for Pharmaceutical Preparations: fifty-fifth report
WHO Expert Committee on Specifications for Pharmaceutical Preparations: fifty-fifth report
Guidelines
Cover publication. Report XCPandrh
Report of the 10th Conference of the Pan American Network for Drug Regulatory Harmonization (PANDRH): The Regulatory Systems in the Health Agenda Post COVID-19. Extraordinary online session 6, 8, and 10 December 2021
Technical reports
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WHO guidelines on good manufacturing practices for blood establishments, Annex 4, TRS No 961
Guidelines
Agenda. 10th Conference of the Pan American Network for Drug Regulatory Harmonization
Meeting Documents
Regulatory reliance principles: concept note and recommendations. Ninth Conference of the Pan American Network for Drug Regulatory Harmonization (PANDRH) (San Salvador, 24 to 26 October, 2018)
Regulatory reliance principles: concept note and recommendations. Ninth Conference of the Pan American Network for Drug Regulatory Harmonization (PANDRH) (San Salvador, 24 to 26 October, 2018)
Technical and scientific products
Post-authorization Surveillance of Medical Products during a Pandemic Emergency, 21 July 2020
Post-authorization Surveillance of Medical Products during a Pandemic Emergency, 21 July 2020
Technical and scientific products
document
CD55.R12 - Access and Rational Use of Strategic and High-cost Medicines and Other Health Technologies
Mandates and Strategies
Strengthening of regulatory systems for medicines in the Americas
Strengthening of regulatory systems for medicines in the Americas
Technical and scientific products
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CE156/INF/8 - F. Health Technology Assessment and Incorporation into Health Systems
Mandates and Strategies
Ethical Criteria for the Promotion, Advertisement, and Publicity of Medicines
PANDRH Series, Technical Document, 12. Ethical criteria for the promotion, advertisement, and publicity of medicines [2013]
Technical and scientific products
Drug-regulation-Americas
PANDRH Technical Document n.10. Requirements for Medicines Registration in the Americas. [2013]
Technical and scientific products
Steering Committee Meeting. Pan American Network on Drug Regulatory Harmonization (PANDRH). Executive Summary. 22-23 November, 2011
Annex 6 . Executive Summary PANDRH Steering Committee Meeting. November 22 and 23, 2011
PANDRH Technical Report Nº 8. Framework for Implementation of Equivalence Requirements for Pharmaceutical Products
PANDRH Technical Report Nº 8 - Framework for Implementation of Equivalence Requirements for Pharmaceutical Products
Technical and scientific products
Rede PARF Documento Técnico No. 9. Boas Práticas da OMS para Laboratórios de Controle de Qualidade de Produtos Farmacêuticos
Rede PARF Documento Técnico No. 9. Boas Práticas da OMS para Laboratórios de Controle de Qualidade de Produtos Farmacêuticos
Technical and scientific products
Presentación - Administración Nacional de Medicamentos, Alimentos y Tecnología Médica: Experiencias en la Regulación de Productos Biológicos
Presentations
Practical guide for procurement planning and management of strategic public health supplies
Technical and scientific products
Download in PDF
CD42/13, Rev. 1 - Pharmaceutical Regulatory Harmonization in the Americas
Mandates and Strategies