Process validation
Preparation of CIP processes
We help you from the application-oriented creation of Cleaning in Process (CIP) cleaning processes, through the definition of analysis methodology, to risk assessment.
Design Transfer - Design Validation & Verification
We accompany you in the planning and execution of design verification and validation up to process qualification.
Reprocessing of medical devices
We support you in the creation and validation of the cleaning and disinfection process, as well as in the preparation of the reprocessing instructions according to ISO 17664.
