Medical Device Innovation Consortium/MDIC’s Case for Quality program today released a whitepaper recasting the Corrective and Preventive Action (CAPA) process as a continuous improvement process and to design a less burdensome process that drives higher product quality and improved patient safety. The whitepaper summarizes the initial findings and recommendations developed by a joint team from MDIC, the medical device industry, strategy consultants, and the FDA, including a proposed framework for risk-based improvement.
For more info and to download whitepaper – https://mdic.org/news/mdic-releases-case-for-quality-capa-process-improvement-whitepaper/?utm_campaign=coschedule&utm_source=twitter&utm_medium=MDIConline