Post-marketing sampling and testing programs for licensed medicinal products: a narrative review-Reference-Cited by-同舟云学术

Post-marketing sampling and testing programs for licensed medicinal products: a narrative review

Published:2022 Issue: Volume:58 Page:
ISSN:2175-9790
Container-title:Brazilian Journal of Pharmaceutical Sciences
language:
Short-container-title:Braz. J. Pharm. Sci.

Author:

Neves Edvaldo Oliveira¹^ORCID,Sales Paloma Michelle de²,Silveira Dâmaris³

Affiliation:

1. Brazilian Health Regulatory Agency (ANVISA), Brazil; University of Brasilia (UnB), Brazil

2. University of Brasilia (UnB), Brazil; Central Laboratory of Public Health of the Federal District (LACEN-DF), Brazil

3. University of Brasilia (UnB), Brazil

Publisher

FapUNIFESP (SciELO)

Link

http://www.scielo.br/scielo.php?script=sci_pdf&pid=S1984-82502022000100597&tlng=en

Reference68 articles.

1. Resolution of the Collegiate Board of Officers RDC nº 37 of July 06, 2009, which deals with the admissibility of foreign pharmacopoeias;Brazilian Federal Register,2009

2. Resolution of the Collegiate Board of Officers RDC nº 49 of November 23, 2010. It approves Brazilian Pharmacopoeia, 5th edition and provides further remedies;Brazilian Federal Register,2010

3. Ordinance nº 452 of February 25, 2013. Approves the Internal Regulations of the Brazilian Pharmacopoeia Commission, revokes Ordinance nº 1015 of July 20, 2011 and gives other provisions;Brazilian Federal Register,2013

4. Anvisa launches drug and device monitoring program: 1,800 samples will be tested,2016

5. Brazilian Pharmacopoeia,2018

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