Process validation is collecting and evaluating data from the process design stage to production, providing scientific evidence that a process can reliably produce high-quality products.
Meetings are organized with the customer about validation at this stage to determine the type of validation they need.
For each validation, the estimated time and human resource planning are meticulously done by our experts. Issues such as worst-case condition analysis of samples and test reports required within the validation scope are discussed with the customer within the plan. The results are reported and included in the customer's system.
Apart from the validation studies continuously offered by DeSia, relevant guidance can be provided upon request if a customer needs a different process validation. Our scope of service is as follows:
- Packaging Process Validation
- Cleaning Process Validation
- Realized for production
- In the case of cleaning in a hospital environment
- Gamma Sterilization Process Validation
- ETO Sterilization Process Validation
- Steam Sterilization Process Validation
- Production Validation (Injection Molding, Filling, etc.)
For more detailed service information, please visit NioReg website.
