Before a product can be assigned to a specific sterilisation process, the first step is to identify the parameters which guarantee the sterility of the particular product at the end of each cycle. This requires performance of a VALIDATION for the product.
Service steps in the preparation stage
- Offer
(Based on your product’s specifications and packaging as well as the expected annual volume, we compile a customized offer for you including a specification of costs for both the validation and regular sterilisation) - Assignment
- VALIDATION
(= The verified development of a process which guarantees consistent success of the process (sterility) based on the same constants each time) - Changeover to routine sterilisation