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07 Oct 2020Ended

QMS vs IVDR: Manufacturer Obligations and Auditing Impact

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upto 100
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Based on previous editions

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07 Oct 2020

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Delve into detailed press kits for information on our work. As the global safety science leader, UL helps companies to demonstrate safety, enhance .. Read more sustainability, strengthen security, deliver quality, manage risk and achieve regulatory compliance. Explore our business intelligence-building digital tools and databases, search for help, review our business information, or share your concerns and questions. The new IVD regulation specifies certain obligations that a manufacturer (and other applicable Economical Operators) cannot miss, including design and manufacturing, risk management, clinical evaluations, UDI, quality management system (QMS), post-market and surveillance activities. This webinar aims to provide clear and unambiguous directions to manufactures in order to meet upcoming expectations and ensure no disruption of availability of medical devices on the CE market.

Speaker
Maurizio La Mura

Maurizio La Mura

IVD Specialist
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UL International Limited

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