Rdc 39/2013 pdf

2019-09-17 00:06

RESOLUO RDC N 9, DE 20 DE FEVEREIRO DE 2015. Dispe sobre o Regulamento para a realizao de ensaios clnicos com medicamentos no Brasil.a Resoluo RDC n 25. independentemente do processo de Certificao. 48 A renovao automtica prevista no art. Art. a qualquer momento. de 9 de dezembro de 1999. de 23 de abril de 2009. sujeitando o infrator s penalidades previstas nesse diploma legal. de 11 de setembro de 2001. rdc 39/2013 pdf

May 08, 2017 Dispe sobre a alterao das Resolues da Diretoria Colegiada RDC n, n, n, n, n, n e n, para a incluso, alterao e excluso de Denominaes Comuns Brasileiras DCB, na lista completa das DCB da Anvisa.

Share (1)RDC COMP. Embed size(px) Link. Share. of 15. Report. All materials on our website are shared by users. If you have any questions about copyright issues, please report us to resolve them. We are always happy to assist you. Related Documents. Share. Transcript This presentation will address the RDC certification on good distribution practices (cGDP) compared with guidelines already recognized worldwide as USP 35 Good Storage and Shipping rdc 39/2013 pdf RESOLUTION RDC No. 39, OF AUGUST 14TH, 2013. Makes provisions on the administrative procedures for granting Good Manufacturing Practice Certification and Good Distribution andor

Resolution RDC No. 167 of July 2, 2004. Article 3 Distributors and storage agents of Medical Devices and In Vitro Diagnostic Devices shall meet the requirements of this Resolution, as applicable. rdc 39/2013 pdf RESOLUO DA DIRETORIA COLEGIADA RDC N 39, DE 14 DE AGOSTO DE 2013. Dispe sobre os procedimentos administrativos para concesso da Certificao de Boas Prticas de Fabricao e da Certificao de Boas Prticas de Distribuio eou Armazenagem A Diretoria ANVISA Health Surveillance National Agency recently published the RDC 39 2013 in August 14th, which changed the administrative procedure to certify good manufacturing practices to medicine, pharmaceutical raw material, medical devices, health care and home care products. NVISA Health Surveillance National Agency recently published the RDC 39 2013 in August 14th, which changed the administrative procedure to certify good manufacturing practices to medicine, pharmaceutical raw material, medical devices, RESOLUO RDC No39, DE 14 DE AGOSTO DE 2013. Dispe sobre os procedimentos administrativos para concesso da Certificao deBoas Prticas

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