A process for Remedial, Corrective and Preventive Action (CAPA) is required by numerous codes of GMP, ISO standards and ICH Guidelines. It is a key tool for achieving continuous improvement.

Verta Life Sciences have the expertise and experience to put an effective CAPA system in place. This process will effectively identify any actual or potential quality or compliance non-conformance. It will evaluate the significance and urgency of actions, control affected material directly or indirectly, implement remedial action, identify the root cause of the problem, and propose the necessary action plan (the CAPA Plan) to prevent a recurrence. In addition it will track actions to completion, and implement documented checks to verify that the required actions have been embedded into working practices, and are effective.