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Journal ArticleOPEN ACCESS

Documentary evidence

Pharmaceutical Technology Europe (2005) 17(2) 46-48
DOI: 10.5040/9798216017509.ch-006
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Abstract

This article looks at the role of document management in the product lifecyle and its pivital contribution to the effective use of CTDs (common technical documents) and e-CTDs (electronic technical documents) when compiling compulsory regulatory submissions. The importance of granularity of data is emphasised.

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APA

Burd, J., & Braun, R. (2005). Documentary evidence. Pharmaceutical Technology Europe, 17(2), 46–48. https://doi.org/10.5040/9798216017509.ch-006

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