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
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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...
Continue ReadingHuma.AI MDR and IVDR Expert Panel Discussion Highlighted the Need for New Machine Learning Solutions to Tackle Post-Market Data
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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...
Continue ReadingHuma.AI Sponsors New EU MDR and IVDR Resource Center for MedTech Regulatory Professionals
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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...
Continue ReadingHow 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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