Quality of medicines: Deficiencies found by Brazilian Health Regulatory Agency (ANVISA) on good manufacturing practices international inspections

Author:

Geyer Andrea Renata CornelioORCID,Sousa Varley Dias,Silveira Dâmaris

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference54 articles.

1. WHO good manufacturing practices for pharmaceutical products: main principles;WHO Tech Rep Ser,2014

2. ANVISA. Resolução RDC no 17 de 16 de abril de 2010. Diário Of da União. 2010;19 abr: 94–110.

3. EU Guidelines for Good Manufacturing Practice for Medicinal Products for Human and Veterinary Use;EudraLex,2012

4. PIC/S. Guide To Good Manufacturing Practice for Medicinal Products. 2017;

5. FDA. Facts About the Current Good Manufacturing Practices (cGMPs) [Internet]. 2015 [cited 28 May 2017] pp. 1–3. Available: http://www.fda.gov/Drugs/DevelopmentApprovalProcess/Manufacturing/ucm169105.htm

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