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Tagged medical-device-safety-and-regulation

State of the Art Literature Review for EU MDR Compliance: How to Get It Right, New Webinar Hosted by Xtalks

Press Release Nov 28, 2018

State of the Art Literature Review for EU MDR Compliance: How to Get It Right, New Webinar Hosted by Xtalks

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EU MDR Strategies: How to Achieve a Market Advantage While Streamlining Regulatory Compliance, New Webinar Hosted by Xtalks Sponsored by Kalypso

Press Release Oct 25, 2018

EU MDR Strategies: How to Achieve a Market Advantage While Streamlining Regulatory Compliance, New Webinar Hosted by Xtalks Sponsored by Kalypso

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How to Ensure Compliance With the New EU Medical Device Regulations: MDR & IVDR, New Webinar Hosted by Xtalks

Press Release Aug 24, 2018

How to Ensure Compliance With the New EU Medical Device Regulations: MDR & IVDR, New Webinar Hosted by Xtalks

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Quality In, Quality Out: Regulatory Drivers of Supplier Quality Management in the Medical Device Industry -- New Webinar Hosted by Xtalks

Press Release Jul 26, 2018

Quality In, Quality Out: Regulatory Drivers of Supplier Quality Management in the Medical Device Industry -- New Webinar Hosted by Xtalks

In this second of a four-part webinar series, the presenter will take a specific and deeper dive into the regulatory requirements for supplier management for the MedTech - medical devices and in-vitro diagnostics - industry. Read More

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