Capa (or Corrective Action and Preventative Action) in the Pharmaceutical Industry: The process of identifying, assessing, and responding to risks and opportunities related to quality and safety in the pharmaceutical industry. Capa is vital for ensuring that products meet all applicable regulatory requirements and standards. This process involves analyzing existing procedures and making necessary adjustments in order to prevent any risk of product failure or other undesired outcomes. Additionally, capa helps maintain product quality through corrective actions, such as correcting health hazards or hazardous conditions before they arise. Ultimately, Capa safeguards consumers by ensuring that pharmaceutical products comply with regulatory and industry standards.