Competent implementation of GMP requirements
The EU GMP guidelines (Good Manufacturing Practice) for human and veterinary pharmaceuticals places enormous requirements on the pharmaceutical industry. Meeting them is a tour de force in terms of time and resources. Extreme care and well-founded technical knowledge are an absolute requirement.
We can support you professionally and competently in the implementation of your GMP requirements, with a great love of detail. COMNOVA GmbH, as a service provider of qualification and validation measures in the pharmaceutical industry, has shown its acumen in numerous projects. Ask for your special know-how and our years of experience!
COMNOVA’s GMP services include:
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Preparation of qualification and validation documents
- Validation master plan
- Risk analyses
- Qualification plans
- Qualification test protocols
- Qualification reports
- Implementation of qualification measures (DQ, IQ, OQ, PQ)
- Performance of measurements (temperature/pressure/humidity, etc.) as part of qualification and requalification measures