An Effective CAPA FDA and CAPA Quality Plan For Easy Implementation, Reducing Defects and Lowering Penalty Costs.
A CAPA plan is a quality management strategy used in the manufacturing and production industries to identify and rectify defects to ensure they won’t repeat again in the future. Once a CAPA plan is implemented, it must illustrate ten objectives to meet the intent of the FDA 21 CFR 820.100 requirement.