InnoScan's Quality System

InnoScan uses its own quality control system described in InnoScan's Quality Manual.

InnoScan's quality control system complies with strict quality guidelines such as the GAMP.

To ensure direct traceability from customer requirements, through InnoScan's analysis to the testing phase, all customer requirements are listed in the 'Project Requirement List'. The list refers back to customer's User Requirement Specification and forward to that document where the requirement is being analysed, and finally tested.
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Commissioning

InnoScan offers standard solutions as well as customer engineering including installation, commissioning and comprehensive qualification documentation. World-wide after sales support is guaranteed with specified reaction pattern.

Validation

All InnoScan's activities are performed in accordance with cGMP recommendations, and a documentation package acceptable to the FDA is available.

InnoScan can offer a full validation package, can participate in the validation, or the customer can choose to do the validation by himself.

The validation can be build directly upon InnoScan's qualification documentation; so many tests will not have to be carried out again, thereby speeding up the validation process significantly.

InnoScan's knowledge of cGMP and validation is the result of many years as developer and constructor of inspection equipment within the pharmaceutical industry.