Developing and validating an aseptic filling process in isolators
A sterile and reproducible aseptic filling process inside isolators must be developed and validated. Valicare experts offers workshops to lead you through this process step by step.
A biodecontamination process development and validation must be planned thoroughly to meet regulatory and customer-specific requirements for the aseptic production process.
To meet these requirements, Valicare isolator experts offer workshops with your responsible parties (e.g. process owners, qualification personnel, QA). The workshop is based on the draft version of a biodecontamination process development plan.
