Scarce quality assurance documentation in major clinical trial registries for approved medicines used in post-marketing clinical trials

BACKGROUND: This research reviewed major Clinical Trial Registries (CTRs) and assessed the availability of fields on quality assurance for approved medicines used as Investigational Medicinal Products (IMPs) in phase IV clinical trials. METHODS: Two reviewers independently assessed CTRs of the Inter...

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Detalles Bibliográficos
Autores principales: Doua, Yorokpa Joachim, Dominicus, Hanneke, Mugwagwa, Julius, Gombe, Suzelle Magalie, Nwokike, Jude
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6460528/
https://www.ncbi.nlm.nih.gov/pubmed/30975193
http://dx.doi.org/10.1186/s13063-019-3277-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6460528/
https://www.ncbi.nlm.nih.gov/pubmed/30975193
http://dx.doi.org/10.1186/s13063-019-3277-8

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