Qualifications and Validations (IQ, OQ) of Pharmaceutical Usage Equipment According to GMP

Qualifications and Validations (IQ, OQ) of Pharmaceutical Usage Equipment According to GMP

Sartorom's technical department offers validation services for equipment used in the pharmaceutical industry in accordance with GLP/GMP requirements and regulations.

Qualification consists of performing specific tests and drawing up the related validation protocols: IQ; OQ for:
– Dissolution systems; disintegration testers; hardness, friability, abrasion, powder flow testers; bulk density testers; R&D equipment;
– autoclaves, incubators, climatic/stability chambers, ovens and freezers;
– materials testing machines;
– weighing apparatus; balances, thermogravimeters;
– titrators, pH meters, oxygen meters, etc.
– laser and video granulometers;
– thermal analysis equipment.