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Displaying results 1 to 2 out of 2
|CTSM & GMP||81%|
|... staff dedicated to the GMP area is able to manage all kinds of trial medication (including check after receipt, storage, manufacturing steps, QP release, dispensation for administration, drug accountability and return / destruction) according to the regulatory requirements. Â CRS guarantees QP release of trial medication according to GMP rules (e.g. EudraLex – Vol. 4, PharmBetrV, and EU Clinical Trials Directive 2001/20/EC). Trial ...|
|Size: 33 K - Created: 18-11-12 - Modified: 20-12-17 11:58
Path: /Services/CTSM & GMP
|In a Nutshell||79%|
|... Comprehensive Service Portfolio Consultancy Project Management Clinical Conduct Monitoring Quality Assurance Clinical Trial Supply Management / QPs Laboratory / Bioanalytical Services by external partners Clinical Data Management Statistics Medical Writing In the following we offer you ...|
|Size: 30 K - Created: 12-08-15 - Modified: 20-12-17 11:58
Path: /CRS/In a Nutshell