Providing expert content and conferences to advance the global #medtech industry.
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Joined June 2009
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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!
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MedTech Intelligence retweeted
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
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MedTech Intelligence retweeted
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/colu…
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.
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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.
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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/feat…
New on MedTech Intelligence - Laying the Groundwork for an AI Breakthrough medtechintelligence.com/feat…
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/feat…
Join us on December 16 for a complimentary webinar: The Benefit and Risk of AI Software in Medical Devices
innovativepublishing.actonso…
Yesterday, the Swiss National Council voted to accept FDA approved, as well as EU/CE Mark approved, medical devices into Switzerland.
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Holmes will begin serving her 135 month (11.25 year) sentence in April 2023. medtechintelligence.com/news…
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
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The $16.6 billion acquisition will bring @Abiomed's breakthough Impella heart pumps into the Johnson & Johnson MedTech portfolio. medtechintelligence.com/news…
The @US_FDA has updated its 2017 guidance, “Developing and Responding to Deficiencies in Accordance with the Least Burdensome Provisions.” medtechintelligence.com/news…
Image integrity is key to publishing reputable and reliable clinical studies. Learn about new tools to help identify duplicate and altered images.
@Proofig
medtechintelligence.com/colu…