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Carpeta PANDRH-Pan American Network for Drug Regulatory Ha

 PAN AMERICAN NETWORK FOR DRUG REGULATORY HARMONIZATION

Categorías

Documentos

pdf Bioequivalence and good manufacturing practices (GMP) in Chile - Verónica Vergara - ISP  Publicado Popular

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VII PANDRH Conference.

pdf Biotechnological Product Work Group  Publicado Popular

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pdf Biotechnological Products Working Group Report. PANDRH. 17 Jun 2010  Publicado Popular

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BIOTECHNOLOGICAL PRODUCTS WORKING GROUP REPORT.PAN AMERICAN NETWORK ON DRUG REGULATORY HARMONIZATION (PANDRH)

Meeting date: 17 June 2010

Place: Punta Cana, Dominican Republic

Objectives

1. To select the main and alternate country coordinators for the working group (WG).

2. To establish short- and middle-term objectives for the WG, as well as to define the chronogram of activities.

3. To establish communication mechanisms.

pdf Biotherapeutic products thematic session  Publicado Popular

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pdf Brazilian System of Medical Devices Regulation - Dirceu Barbano -ANVISA  Publicado Popular

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VII PANDRH Conference.

pdf Call for Projects VIII CPANDRH. Proposal submission  Publicado Popular

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pdf CARICOM Challenges  Publicado Popular

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pdf Challenges when implementing guidelines for biosimilars - Agnes Klein -CERB  Publicado Popular

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VII PANDRH Conference.

pdf COFEPRIS cooperation with El Salvador  Publicado Popular

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VII PANDRH Conference.  

pdf Comite ejecutivo red parf jul 2017  Publicado Popular

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comite-ejecutivo-red-parf-jul-2017.pdf

Minuta de la Reunión virtual del Comité Directivo Red PARF.  18 de julio del 2017.

pdf Consulta pública de los contenidos del Guía para el Manual del Investigador (enero 2011)  Publicado Popular

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La Red Panamericana para la Armonización de Regulación Farmacéutica (PARF), Grupo Técnico Ensayos Clínicos,  le invita a participar de la consulta pública de los contenidos de la Guía para el Manual del Investigador
 
Fecha de Inicio: 28 de enero de 2011
Fecha de Término: 28 de marzo de 2011

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pdf Cpp proyecto eng feb 2018  Publicado Popular

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cpp-proyecto-eng-feb-2018.pdf

 

Title: Assessing CPP requirements for drug registration processes in the Region of the Americas towards more timely access to medicines and more convergent regulatory approaches.
Cross-cutting areas: Authorization, Registration and Licensing of products and facilities and Good Regulatory Practices and Regulatory Sciences

Initiator: Latin America Federation of the Pharmaceutical Industry - FIFARMA

pdf Decision tree for the implementation of the Guideline for Good Manufacturing Practices Inspection.  Publicado Popular

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PANDRH WG/GMP. V Conference of the Pan American Network for Drug Regulatory Harmonization (PANDRH). Buenos Aires, Argentina. November 17th – 19th, 2008.  Decision tree for the implementation of the Guideline for Good Manufacturing Practices Inspection

The implementation of this Guideline supports compliance with the WHO GMP standards according to Report #32 and updates until 2003, date of preparation of the Guideline.

The Guide for GMP Inspection was adopted by PANDRH at the IV Conference. 

 The working group on GMP (WG/GMP), considering the differences among the levels of development of the pharmaceutical industry in the Region and the political and economic realities of the countries in the Americas, considered it necessary to define a Decision Tree to guide the countries in applying these standards and to set priority of the actions to follow. The document is aimed to guide the NRA and the pharmaceutical industry in prioritizing the requirements of the standards. However, it is estimated that the application of the priorities as they are presented in this document have the flexibility that the national situation requires.

This document is based on a proposal carried out in Venezuela and on resolution 01267 of 2/8/2001 from Colombia.

The document, prepared by the PANDRH WG/GMP members has been approved during their VI meeting (March 2006) as draft for public opinion. It is currently available in the webpage of PANDRH. In compliance of PANDRH process, all comments from the public will be reviewed by the WG/GMP in preparation of the final version.

pdf El salvador info pais ix cparf  Publicado Popular

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ix-cparf-inf-spa.pdf

pdf Elluminate December 17, 2010  Publicado Popular

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pdf Elluminate December 17th, 2010  Publicado Popular

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pdf Elluminate January 14th, 2011  Publicado Popular

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pdf Elluminate November 11th, 2010  Publicado Popular

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pdf Elluminate September 17th, 2010  Publicado Popular

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pdf Establishing Clinical Similarity for Similar Biotherapeutic Products – The Concept of Sensitive Populations -Thomas Schreitmueller - FIFARMA  Publicado Popular

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VII PANDRH Conference.

pdf Ethical Criteria for Promoting, Advertising, and Publicizing Pharmaceuticals  Publicado Popular

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pdf Evidence-based development of the Caribbean Pharmaceutical Policy  Publicado Popular

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pdf Executive Summary- PANDRH Steering Committe. November 2011  Publicado Popular

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pdf Exigences harmonisées pour l’homologation des vaccins Dans la Région des Amériques et Guide d’application  Publicado Popular

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pdf Exigences harmonisées pour l’homologation des vaccins Dans la Région des Amériques et Guide d’application  Publicado Popular

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Exigences harmonisées pour l'homologation des vaccins Dans la Région des Amériques et Guide d'application

RPHRP Document technique

No. 1 Réseau panaméricain d'harmonisation de la réglementation pharmaceutique

Groupe de travail sur les vaccins

pdf Final minutes PANDRH January 15  Publicado Popular

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Final Minutes PANDRH - January 15

pdf Formulario Propuesta de Requisitos Harmonizados  Publicado Popular

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pdf Formulary - Health authorities Medicine Counterfeiting  Publicado Popular

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health-authorities-medicine-counterfeiting-formulary-2011.doc

pdf Formulary - Model for a Focal Point Network to Combat Counterfeit Medicines  Publicado Popular

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pdf Formulary - Promoting Pharmaceutical  Publicado Popular

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pdf Formulary Use of Placebos  Publicado Popular

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pdf Formulary-Clinical Studies in Pediatric  Publicado Popular

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pdf Framework for Implementation of Equivalence Requirements for Pharmaceutical Products. Proposal  Publicado Popular

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Pan American Network on Drug Regulatory Harmonization Working Group on BE. Framework for Implementation of Equivalence Requirements for Pharmaceutical Products. Proposal to be submitted to the V Conference for Drug Regulatory Harmonization. October 2008

pdf Framework for implementation of equivalence requirements for pharmaceutical products. Document appr  Publicado Popular

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Pan American Network on Drug Regulatory Harmonization.Working Group on BE. Framework for implementation of equivalence requirements for pharmaceutical products.  Document approved in the V Conference for Drug Regulatory Harmonization. Buenos Aires, Argentina. 17 - 19 November, 2008.

pdf Good Clinical Practices Work Group  Publicado Popular

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pdf Good Laboratory Practices  Publicado Popular

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pdf Good Practices Self-Evaluation Guide for National Pharmaceutical Control Laboratories  Publicado Popular

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PAHO.GOOD PRACTICES SELF-EVALUATION GUIDE FOR NATIONAL PHARMACEUTICAL CONTROL LABORATORIES

pdf Governance Models of other networks: APEC and IMDRF - Mike Ward Health Canada  Publicado Popular

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VII PANDRH Conference.

pdf Guide for Conducting Clinical Studies in Pediatric Populations  Publicado Popular

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pdf Guidelines to be Considered By Health Authorities in Cases of Suspected Medicine Counterfeiting  Publicado Popular

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pdf II Workshop on Medicines Regulation in the Caribbean Region: CURRENT STATUS OF PAN AMERICAN NETWORK  Publicado Popular

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II Workshop on Medicines Regulation in the Caribbean Region: CURRENT STATUS OF PAN AMERICAN NETWORK FOR DRUG REGULATORY HARMONIZATION (PANDRH)

pdf Implementation of bioequivalent medicines regulation - Laura Castanheira - ANVISA  Publicado Popular

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VII PANDRH Conference.

pdf Implementation of WHO standards for regulatory evaluation of similar biotherapeutic products SBPs - Ivana Knezevic - WHO  Publicado Popular

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VII PANDRH Conference.

pdf Introduction for SSFFC medical products: global and regional perspectives  Publicado Popular

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VII PANDRH Conference.

pdf IX CPANDRH important information, logistics, visa information, taxi service, hotels  Publicado Popular

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Información- reglamentofarma-INGLES- final.pdf

IX CPANDRH important information, logistics, visa information, taxi service, hotels, registration, contacts

pdf IX CPANDRH Participants registration form.  Publicado Popular

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Registration-Form-IX-CPANDRH.docx

IX CPANDRH Participants registration form.

pdf Ix cparf agenda 2018 spa  Publicado Popular

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ix-cparf-agenda-2018-spa.pdf

Agenda. IX Conferencia Panamericana para la Armonización de la Reglamentación Farmacéutica (CPARF) San Salvador, El Salvador 24 al 26 de octubre de 2018 “Contribuciones de la armonización regulatoria en el logro de salud para todos” Conmemorando 20 años de la Red PARF y 40 años de ALMA ATA

pdf Lessons learned from international effective cooperation agreements TECHPHARM - Maryam Karga-Hinds -Barbados Drug Services  Publicado Popular

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VII PANDRH Conference  

pdf Level of adoption and implementation of PANDRH 7th technical document - Patricia Saidón  Publicado Popular

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VII PANDRH Conference.

pdf Logistics VI Conference  Publicado Popular

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