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February 29, 2024 - March 01, 2024 / Europe

Join the two-day workshop on US FDA Pre-Submissions led by Lorry Weaver and Christie Hughes

In this 2-day workshop in Rotterdam, The Netherlands, our US FDA experts Lorry Weaver and Christie Hughes will review the multiple types of pre-submissions, or Q-submissions, available to manufacturers and how to leverage these to reduce the time and costs to bring medical devices to market in the U.S.
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March 07, 2024 - March 07, 2024 / Europe

Join the workshop FDA Fundamentals at Briskr Netherlands

Meet Lorry Weaver, our FDA expert from the US at Noviotech Campus Nijmegen, The Netherlands and learn the key expectations and processes required to achive FDA clearance of your device to the US market.
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March 19, 2024 - March 19, 2024 / Europe

Free Webinar | Extension to the IVDR what does it mean for you?

Join the free webinar on the 19th of March which brings the experts together from Notified Bodies, industry, and the legal sector to deliver a comprehensive update on what this latest extension to the IVDR means for you.
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March 21, 2024 - March 21, 2024 / Canada

Free Webinar | Medical Device Registration in Canada

How to enter the Canadian medical device market and meet regulatory compliance.
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April 18, 2024 - April 25, 2024 / Virtual

Virtual Training: PRRC | Person Responsible for Regulatory Compliance

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