|Articles|February 1, 2005
Pharmaceutical Technology Europe
- Pharmaceutical Technology Europe-02-01-2005
- Volume 17
- Issue 2
Documentary Evidence
Author(s)Jonathan Burd, Romuald Braun
A look at the role of document management in the product life-cycle and how this can lead to the effective use of CTDs and e-CTDs when compiling compulsory regulatory submissions...
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Monitoring Granulation Drying Using Near-Infrared Spectroscopyalmost 21 years ago
Process Considerations During API Developmentalmost 21 years ago
The Introduction of GMP for APIs in the European Unionalmost 21 years ago
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