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Did you know that every year since 2010 the #1 reason medical device companies receive FDA 483’s is poor CAPA procedures? Here’s a best practice guide to help you implement a best practice approach to CAPA while avoiding the common pitfalls → https://blog.greenlight.guru/corrective-action-and-preventive-action-capa-medical-devices  Ultimate Guide to Corrective and Preventive Action (CAPA) for Medical DevicesHow to implement and maintain a risk-based CAPA process while avoiding the most common pitfalls at your medical device company. source: https://www.linkedin.com/groups/78665/78665-6332737576742588416 Marked as spam
 Posted by Asked on November 5, 2017 12:00 am
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