Download or read book WHO Expert Committee on Specifications for Pharmaceutical Preparations written by and published by World Health Organization. This book was released on 2021-04-26 with total page 324 pages. Available in PDF, EPUB and Kindle. Book excerpt: The Expert Committee on Specifications for Pharmaceutical Preparations works towards clear, independent and practical standards and guidelines for the quality assurance of medicines and provision of global regulatory tools. Standards are developed by the Expert Committee through worldwide consultation and an international consensus-building process. The following new guidance texts were adopted and recommended for use: Guidelines and guidance texts adopted by the Expert Committee on Specifications for Pharmaceutical Preparations; Points to consider when including Health Based Exposure Limits (HBELs) in cleaning validation; Good manufacturing practices: water for pharmaceutical use; Guideline on data integrity; WHO/United Nations Population Fund recommendations for condom storage and shipping temperatures; WHO/United Nations Population Fund guidance on testing of male latex condoms; WHO/United Nations Population Fund guidance on conducting post-market surveillance of condoms; WHO “Biowaiver List”: proposal to waive in vivo bioequivalence requirements for WHO Model List of Essential Medicines immediate-release, solid oral dosage forms; WHO Certification Scheme on the quality of pharmaceutical products moving in international commerce; Good reliance practices in the regulation of medical products: high-level principles and considerations; and Good regulatory practices in the regulations of medical products. All of the above are included in this report and recommended for implementation.

Download or read book Bonnes pratiques de fabrication pour les fabricants et les importateurs de drogues written by Canada. Health Protection Branch and published by Health Protection Branch = Direction générale de la protection de la santé. This book was released on 1982 with total page 96 pages. Available in PDF, EPUB and Kindle. Book excerpt: Ce guide porte sur les exigences de "bonnes pratiques de fabrication" pour la production et l'importation de drogues d'application humaine ou vétérinaire. Il porte sur le Titre 2 des Règlements sur les aliments et drogues émis par Décret C.P. 1982-1535.

Download or read book Les bonnes pratiques de fabrication dans l industrie pharmaceutique written by Josée Bouchard (Spécialiste de la gestion) and published by . This book was released on 2022 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: "Édition courante qui comprend les exigences des bonnes pratiques de fabrication européennes (Eudralex et Agence nationale de sécurité du médicament et des produits de santé [ANSM]), canadiennes (Santé Canada) et américaines (Food and Drug Aministration [FDA]), incluant les récentes exigences liées à l’intégrité des données. Cet ouvrage reflète les courants modernes en gestion de la qualité en production pharmaceutique et les attentes des agences réglementaires concernant la fabrication, l’emballage, l’analyse, l’entreposage et la distribution des médicaments à usage humain ou vétérinaire. Il cerne les éléments essentiels à la production de médicaments de qualité. Ainsi, ce volume présente les connaissances de base et les principes fondamentaux de l’application des bonnes pratiques de fabrication durant la production manufacturière de produits thérapeutiques. Il permet de se familiariser avec les concepts afin de mieux interpréter l’essentiel des lignes directrices, en considérant les enjeux, les défis et les obstacles tant sur le plan de la conformité que sur celui de l’efficacité dans leur application. Des illustrations, des exemples et des exercices accompagnent le contenu de chaque chapitre."--Page 4 de la couverture

Download or read book Les bonnes pratiques de fabrication dans l industrie pharmaceutique written by Josée Bouchard (spécialiste en gestion de la qualité système).) and published by . This book was released on 2022 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Download or read book D veloppement et valuation du m dicament written by Philippe Lazar and published by . This book was released on 1987 with total page 550 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Download or read book Journal Mondial de Pharmacie written by and published by . This book was released on 1972 with total page 258 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Download or read book Bulletin of the World Health Organization written by World Health Organization and published by . This book was released on 1993 with total page 536 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Download or read book SCAD Bulletin written by and published by . This book was released on 1990 with total page 738 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Download or read book Mondes en d veloppement written by and published by . This book was released on 1996 with total page 428 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Download or read book Les aspects microbiologiques de la fermentation malolactique written by and published by . This book was released on 1993 with total page 94 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Download or read book Current Catalog written by National Library of Medicine (U.S.) and published by . This book was released on with total page 1712 pages. Available in PDF, EPUB and Kindle. Book excerpt: First multi-year cumulation covers six years: 1965-70.

Download or read book Annali dell Istituto superiore di sanit written by and published by . This book was released on 1975 with total page 406 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Download or read book National Library of Medicine Current Catalog written by National Library of Medicine (U.S.) and published by . This book was released on 1987 with total page 1752 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Download or read book Vaccination Animale written by Paul-Pierre Pastoret and published by . This book was released on 2007 with total page 236 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Download or read book Science and Technology in the Transformation of the World written by Anouar Abdel-Malek and published by . This book was released on 1982 with total page 510 pages. Available in PDF, EPUB and Kindle. Book excerpt: references; project on socio-cultural development alternatives in a changing world

Download or read book Dictionary of Pharmaceutical Medicine written by Gerhard Nahler and published by Springer Science & Business Media. This book was released on 2013-06-29 with total page 186 pages. Available in PDF, EPUB and Kindle. Book excerpt: This dictionary is aimed primarily at the beginners entering the new discipline of Pharmaceutical Medicine, an area comprising aspects of toxicology, pharmacology, pharmaceutics, epidemiology, statistics, drug regulatory and legal affairs, medicine and marketing. But also more experienced colleagues in departments engaged in clinical development as well as researchers and marketing experts in the pharmaceutical industry will find concise and up-to-date information. The book is completed by a list of a about 1000 abbreviations encountered in pharmaceutical medicine and a compilation of important addresses of national and international health authorities.

Download or read book Pharmaceutical Prices in the 21st Century written by Zaheer-Ud-Din Babar and published by Springer. This book was released on 2014-12-05 with total page 410 pages. Available in PDF, EPUB and Kindle. Book excerpt: This book provides an overview of the global pharmaceutical pricing policies. Medicines use is increasing globally with the increase in resistant microbes, emergence of new treatments, and because of awareness among consumers. This has resulted in increased drug expenditures globally. As the pharmaceutical market is expanding, a variety of pharmaceutical pricing strategies and policies have been employed by drug companies, state organizations and pharmaceutical pricing authorities.