Documentary Evidence

Article

Pharmaceutical Technology Europe

Pharmaceutical Technology EuropePharmaceutical Technology Europe-02-01-2005
Volume 17
Issue 2

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...

External Link - article-147748.pdf

Articles in this issue
Monitoring Granulation Drying Using Near-Infrared Spectroscopy
Process Considerations During API Development
The Introduction of GMP for APIs in the European Union
Times They Are A-changing
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