- Validation and re-validation are critical, multi-layered processes that ensure every facet of pharmaceutical manufacturing consistently delivers products that meet qulaity standards and requirements.
- For a seamlessly effective experience, DESA develops and deploys a comprehensive validation plan and traceability matrix with tremendously insightful and detailed design specifications, assuring adherence through each phase of execution.
- Qualification and re-qualification are imperative in pharmaceutical manufacturing. These intricate, multilayered processes systematically evaluate equipment, utilites, facilities, materials and shipping.
- Additional, forensic investigations and media simulations help ensure that every system and product meets the latest regulatory standards of safety, efficacy and quality.
- Throughout the multi-phase development process, we endeavor to design, improve and deliver the highest quality pharmaceutical and medical devices with the latest advanced manufacturing processes, augmented by our experience with the intricacies involved.