All documentation is subjected to a version check and an amendment check. At the beginning, the Quality Plan (QP) is produced in close consultation with the customer, it determines the tests and the test schedule to be completed for qualification.
- DQ: Design qualification
- IQ: Installation qualification
- OQ: Operational qualification
- PQ: Performance qualification
All validation and qualification operations, results and alterations are summarised in the final document, the Quality Report (QR). Additionally, it contains references to all test reports and raw data.
The prospective Computer System Validation (CSV) encompasses the specification, production, testing and validation of software and we complete it in accordance with the GAMP guideline (Good Automation Manufacturing Practice). The "21 CFR Part 11" law of the American health authorities is taken into full consideration.
Further information on
GAMP
Further information on
21 CFR Part 11