• What happens when something goes wrong? CAPAs for Equipment

    1 month ago - By PSC Biotech

    What is a CAPA? It is the acronym given to Corrective and Preventative Action , as defined by the FDA. A CAPA is triggered when a product, process, or documentation has a non-compliance issue. CAPAs can be triggered from small or large issues. A small issue might be repeated product loss from intermittent equipment error. Whereas a more significant CAPA trigger results from errors in product packaging that trigger a Form 483 from the FDA.
    If you are in the pharmaceutical, biotechnology, or healthcare industries, you need proper CAPA support to bring your systems back to an acceptably...
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