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Topic: Pmi

Is IVDR Wearing You Down? A Webinar Reviews 2022 for IVD Manufacturers
By Sean Smith on December 9, 2022

IVDR 2022: The Year In Review Webinar with IVD Insider Carlos Galamba Is the In Vitro Diagnostic Regulation (IVDR) wearing you down? If so, you’re...

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Machine Learning and the Future of Systematic Literature Review
By Lana Feng, Ph.D. on April 21, 2022

Laurie Mitchell, President of Criterion Edge, recently sat down for an interview to discuss the uses and benefits of Systematic Literature Review...

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Huma.AI MDR and IVDR Expert Panel Discussion Highlighted the Need for New Machine Learning Solutions to Tackle Post-Market Data
By Sean Smith on April 4, 2022

Last week, Huma.AI sponsored a webinar with MedTech Intelligence covering the challenges and opportunities created for post-market intelligence by EU...

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Huma.AI Sponsors New EU MDR and IVDR Resource Center for MedTech Regulatory Professionals
By Lana Feng, Ph.D. on April 1, 2022

Huma.AI has announced the launch of a new EU MDR and IVDR Resource Center on MedTech Intelligence (MTI). The MTI Resource Center is a free community...

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How to Develop an Agile Post-Market Surveillance Framework
By Emily Piernick on March 25, 2022

The resources required for compliance with the European Union Medical Device Regulation (EU MDR) and the In Vitro Diagnostic Regulation (EU IVDR)...

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