Quality Control of Medicines Documents
16 Oct 2023
Market research to identify and analyze opportunities to produce strategic health technologies in Latin America and the CaribbeanTechnical and Scientific Products
31 Dec 2022
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
4 Feb 2022
WHO guidelines on good manufacturing practices for blood establishments, Annex 4, TRS No 961Guidelines
3 Dec 2021
Agenda. 10th Conference of the Pan American Network for Drug Regulatory HarmonizationMeeting Documents
1 Mar 2021
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
21 Jul 2020
Post-authorization Surveillance of Medical Products during a Pandemic Emergency, 21 July 2020Technical and Scientific Products
7 Oct 2016
CD55.R12 - Access and Rational Use of Strategic and High-cost Medicines and Other Health TechnologiesMandates and Strategies
9 May 2016
Strengthening of regulatory systems for medicines in the AmericasTechnical and Scientific Products
24 Mar 2016
Recommendations of the Expert Committee for the Selection and inclusion of Medicines in the PAHO’s Strategic Fund 2015.Technical Reports
25 May 2015
CE156/INF/8 - F. Health Technology Assessment and Incorporation into Health SystemsMandates and Strategies
11 Dec 2013
PANDRH Series, Technical Document, 12. Ethical criteria for the promotion, advertisement, and publicity of medicines [2013] Technical and Scientific Products
24 Jun 2013
PANDRH Technical Document n.10. Requirements for Medicines Registration in the Americas. [2013]Technical and Scientific Products
24 Jun 2011
PANDRH Technical Report Nº 8 - Framework for Implementation of Equivalence Requirements for Pharmaceutical ProductsTechnical and Scientific Products
2 Jun 2011
Rede PARF Documento Técnico No. 9. Boas Práticas da OMS para Laboratórios de Controle de Qualidade de Produtos FarmacêuticosTechnical and Scientific Products
2 Jul 2008
Presentación - Administración Nacional de Medicamentos, Alimentos y Tecnología Médica: Experiencias en la Regulación de Productos BiológicosPresentations
6 Jun 2006
Practical guide for procurement planning and management of strategic public health suppliesTechnical and Scientific Products
13 Sep 2000
CD42/13, Rev. 1 - Pharmaceutical Regulatory Harmonization in the AmericasMandates and Strategies