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|CTSM & GMP||81%|
|... with classification areas as follows: ‘Quarantine’, ‘Free for use’ or ‘Barred’. The air-conditioned GMP area is monitored every working day. Temperature and humidity are recorded by a data logger which activates a central alarm if the temperature deviates beyond a set limit. Thorough accountability is performed for all trial medications. The production room is designed according to clean ...|
|Size: 33 K - Created: 18-11-12 - Modified: 14-12-18 17:16
Path: /Services/CTSM & GMP