Documentation and Records: Harmonized GMP Requirements

‘If it’s not written down, then it didn’t happen!’ The basic rules in any good manufacturing practice (GMP) regulations specify that the pharmaceutical manufacturer must maintain proper documentation and records. Documentation helps to build up a detailed picture of what a manufacturing function has...

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Detalles Bibliográficos
Autores principales: Patel, KT, Chotai, NP
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications 2011
Materias:
Quality Assurance
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3122044/
https://www.ncbi.nlm.nih.gov/pubmed/21731360
http://dx.doi.org/10.4103/0975-1483.80303

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3122044/
https://www.ncbi.nlm.nih.gov/pubmed/21731360
http://dx.doi.org/10.4103/0975-1483.80303

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