| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1086160 | Le Pharmacien Hospitalier et Clinicien | 2016 | 5 Pages |
Abstract
The BRC is a regulatory document essential for IDÂ dispensing. However, it is not usually provided upfront but often after asking and chasing the promoter. Checking the consistency of the document with the protocol and labelling of ID is an essential prerequisite to any dispensation in clinical trial.
Keywords
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Pharmacology, Toxicology and Pharmaceutics (General)
Authors
C. Le Roy, B. Deluca-Bosc, S. Honoré,