MedTech Intelligence

Join us in Washington, DC, November 7-8 as we take a closer look at how AI/ML is impacting quality management systems and processes, and learn how Pfizer is harnessing these new technologies. eventleaf.com/e/MedTechAdvan… @Axendia

Join keynote speakers Michael Schiller, Sr Director, Supply Chain at @AHRMM, and Alan Edwards, VP Supply Chain Solutions Group at Mary Washington Healthcare, at the Supply Chain Intelligence Summit in November: eventleaf.com/e/MedTechAdvan… @axendia

We are thrilled to share that Robert Nuñez will be joining us at the MedTech Supply Chain Summit in November. We look forward to seeing you there: eventleaf.com/e/MedTechAdvan…

Join members of Ethicon, Pfizer and FDA at the MedTech Advanced Manufacturing and Supply Chain Summits coming to Washington, DC, in November! medtechintelligence.com/column/join-jj…

Adoption of both #SBOM and the @ISA_Automation ISA /IEC 62443 series of standards can help ensure that medical devices breeze through FDA’s premarket submission process and can be operated securely by end users. @MTI_Editor #cybersecurity #otsecurity medtechintelligence.com/feature_articl…

Join our webinar with @MTI_Editor for a discussion of why regulatory strategy should be a competitive advantage for today's #medtech companies. hubs.li/Q01JZVB20

The MedTech Regulatory Intelligence Summit will take place May 16-17 in Washington, DC. Early bird registration is now open. medtechintelligence.com/column/develop…

Mauricio Uribe of @KnobbeMartens discusses the doctrine of assignor estoppel; when it may or may not not apply and what inventors and medtech companies should do to ensure they comply with the court's most recent clarification of the doctrine. medtechintelligence.com/feature_articl…

@AvaniaClinical has acquired MAXIS, a medical technology development service provider with expertise in preclinical engineering, design validation and verification, regulatory affairs, field clinical services, and trial management. medtechintelligence.com/news_article/c…

Jack Cronenwett, MD, shares four areas where medical device manufacturers can strengthen value by partnering with a registry to gather real-world evidence for evaluation of medical devices. medtechintelligence.com/column/how-rea…

Join us on March 14-15 in Washington, DC, at we take a closer look at what’s next—and what’s holding us back—on the road to a truly connected healthcare system. eventleaf.com/e/MTIConnected…

Connected sensors can bring a broader patient base to clinical trials, but finding the correct device for your target endpoints is key. @medableinc's Andrew Mackinnon covers key considerations. medtechintelligence.com/feature_articl…

New on MedTech Intelligence - Laying the Groundwork for an AI Breakthrough medtechintelligence.com/feature_articl…

Stuart Long, CEO of InfoBionics, discusses new innovations as well as what’s needed to move connected care and remote patient monitoring to the next level of adoption. medtechintelligence.com/feature_articl…

Join us on December 16 for a complimentary webinar: The Benefit and Risk of AI Software in Medical Devices innovativepublishing.actonsoftware.com/acton/fs/block…

Yesterday, the Swiss National Council voted to accept FDA approved, as well as EU/CE Mark approved, medical devices into Switzerland. medtechintelligence.com/news_article/s…

Holmes will begin serving her 135 month (11.25 year) sentence in April 2023. medtechintelligence.com/news_article/t…

By applying HFE principles early on, packaging design can evolve beyond usability evaluations in product development to ensure a better user experience and safe execution, says Sean Hagen of @BlackHagenDesgn @Bluediin medtechintelligence.com/column/why-hum…

The $16.6 billion acquisition will bring @Abiomed's breakthough Impella heart pumps into the Johnson & Johnson MedTech portfolio. medtechintelligence.com/news_article/j…

The @US_FDA has updated its 2017 guidance, “Developing and Responding to Deficiencies in Accordance with the Least Burdensome Provisions.” medtechintelligence.com/news_article/f…