Documents
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
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
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
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