|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...
Advertisement
Articles in this issue
over 21 years ago
Monitoring Granulation Drying Using Near-Infrared Spectroscopyover 21 years ago
Process Considerations During API Developmentover 21 years ago
The Introduction of GMP for APIs in the European Unionover 21 years ago
Times They Are A-changingAdvertisement
Related Content
Advertisement
Advertisement
Advertisement
Trending on Pharmaceutical Technology
1
Seventeen Peptide Guidance Revised: What Developers Need to Know
2
Quality and Regulations eBook July 2026
3
Midyear 2026 Industry Report: Taking Stock of Pharma Manufacturing, AI, and Regulatory Trends
4
Modern Control Strategies for Biopharmaceutical Monitoring
5