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

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Description

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.