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Drug Master File Document Production Software In Europe
3 software items found
by:N-SIDE based inLouvain-La-Neuve, BELGIUM
End-to-end clinical trial supply chain visibility and optimization. Enable ambitious clinical plans through an optimal supply ...
by:MasterControl, Inc based inSalt Lake City, UTAH (USA)
OOS Software to Automate Out of Specification (OOS) Processes to Comply with FDA CGMPs and 21 CFR Part 211 and Part 820 Regulations. In the FDA environment, specifications are essential in maintaining quality. CGMP regulations for finished pharmaceuticals (21 CFR Parts 210-211) and medical devices (21 CFR Part 820) require strict conformance to approved specifications which can be acheived easily ...
by:N-SIDE based inLouvain-La-Neuve, BELGIUM
Optimize end-to-end production planning from DS to IMP. The N-SIDE Production App gives you unprecedented flexibility to optimize manufacturing for your clinical projects, from drug substance (DS) to drug product (DP) to investigational medicinal product (IMP). Use the Production App to build and maintain an optimal clinical production plan that accounts for your specific constraints. Respond ...