Integrating Risk Management & CAPA: How to Supercharge Your Medical Device Quality
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Integrating Risk Management & CAPA: How to Supercharge Your Medical Device Quality
Did you know that over 60% of medical device quality issues stem from ineffective CAPA processes, and nearly half of all FDA warning letters cite deficiencies in risk management? CAPA and risk management are not just regulatory requirements but essential components of ensuring product safety and compliance in the medical device industry ...
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