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|CDM & STAT||81%|
|... treatment observation in full compliance with CFR 21, part 11 (as confirmed by internal GAMP4 and GAMP5 validation). Data Management The highly qualified and motivated team has more than three decades of experience in services related to submitting clients’ drugs for regulatory approval and ... Management & Biometrics Department can of course be contracted separately. Able to handle large quantities of data efficiently, CRS’s highly-|
|Size: 31 K - Created: 18-11-12 - Modified: 02-08-19 10:27
Path: /Services/CDM & STAT
|... GMP-certified facilities are located in-house to enable the preparation, packaging and labelling of trial medication under the supervision of a qualified expert. History The unit was originally established in 1992 as an independent, privately owned, Phase I CRO by Dr. Torben Thomsen and a ...|
|Size: 32 K - Created: 18-11-12 - Modified: 02-08-19 10:27