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| | ISO 13485 Training (20th May 25 at 6:58am UTC) | {if:0}  {/if}{if:0} {/if}{if:0} {/if} | ISO 13485 is an international standard that specifies the requirements for a quality management system in the medical devices industry. Lead auditors play a crucial role in ensuring that medical device manufacturers comply with the requirements of ISO 13485 and consistently produce safe and effective products.
iso 13485 lead auditor training
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