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. https://t.co/rMJqaB7ETv
@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: https://t.co/rMJqaB7ETv @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: https://t.co/rMJqaB7ETv
Join members of Ethicon, Pfizer and FDA at the MedTech Advanced Manufacturing and Supply Chain Summits coming to Washington, DC, in November!
https://t.co/a3DIzKN60w
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
https://t.co/viuHmKGV2V
Join our webinar with @MTI_Editor for a discussion of why regulatory strategy should be a competitive advantage for today's #medtech companies. https://t.co/d6qLR2LdsD
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.
https://t.co/RiFczhNWRq
@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.
https://t.co/zzFDJ83t9L
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.
https://t.co/0oMnnG1ita
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.
https://t.co/10P0UqRPGK
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. https://t.co/h0WE6Vdi53
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.
https://t.co/Wx9L51aBwX
Yesterday, the Swiss National Council voted to accept FDA approved, as well as EU/CE Mark approved, medical devices into Switzerland.
https://t.co/TkSJDD02m2
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
https://t.co/gWSX6Cavi7
The $16.6 billion acquisition will bring @Abiomed's breakthough Impella heart pumps into the Johnson & Johnson MedTech portfolio. https://t.co/lHy945b43C
The @US_FDA has updated its 2017 guidance, “Developing and Responding to Deficiencies in Accordance with the Least Burdensome Provisions.” https://t.co/ZLIlX5j5ZL