Validation
Safety. Consistency. Quality.
Pharmaceutical validation and re-validation are critical, multi-layered processes that ensure every facet of pharma manufacturing consistently delivers products that meet quality standards and requirements. For a seamlessly effective experience, DESA develops and deploys a comprehensive plan and traceability matrix with tremendously insightful and detailed design specifications, assuring adherence through each phase of execution.
Our strategic risk-based approach prioritizes performance and functionality with rigorous pharmaceutical testing, analysis and documentation, demonstrating exceptional precision, specificity and robustness. Through validation expertise, we ensure products and processes fulfill intended specifications, yielding safe and effective pharmaceutical products in absolute regulatory compliance.
Validation and re-validation of equipment and quality control instruments involve a structured approach to confirm that all equipment functions as intended throughout its lifecycle.
Utilities Validation, which encompasses the infrastructure of systems, liquids, gases and other compounds engaged in manufacturing, is essential to ensure they meet stringent quality and safety standards. Regular re-validation processes are implemented to confirm there liability and suitability of these systems for their intended use in manufacturing and laboratory environments.
Facilities validation verifies that environmental controls within pharmaceutical testing laboratories, clean room environments and manufacturing facilities operate effectively to uphold the required production conditions. We perform periodical re-validation to address facility or operational changes, ensuring continued regulation compliance.
Material validation and re-validation are crucial for verifying stability conditions for product safety and efficacy and continued compliance with established standards for unyielding product integrity.
ShippingValidation of shipping methods ensures pharmaceutical products are transported under controlled conditions in a manner that maintains their integrity, while re-validation efforts confirm that shipping practices remain effective in protecting product quality throughout distribution.