Zynex Medical’s Post

Do you think innovation in the EU is limited? I think this worth being discussed.. Stay tuned for our upcoming #DigitalDialogues Vol. 5 in a new form. Andrea Lauterbach will interview our experts on several topics also including #cybersecurity #AI #MRIsafety #biocompatibility and many more.

Start up your engines for Day 3 of #InnovationSF23. Jennie Xue (Guggenheim Partners) takes the stage to discuss Medical Device M&A and Public Market Perspectives. This keynote is full of takeaways to make you aware of the greater #medtech market as we move forward. For Experts. By Experts: bit.ly/3QvOw6I

The third edition of The Quarterly Connection, powered by Global Interconnect, provides updates and insights on the medical device industry and the Gii company throughout the third quarter of 2023. #medicaldevice #medicaldevices #newsletter

Curious about the Breakthrough Devices Program? Wondering if it's the right fit for your organization? Parexel’s MedTech Regulatory Strategy and Health Advances MedTech consulting teams have conducted research on the challenges and benefits of the designation and are excited to share those learnings with others in the medical device industry. Join our panel of regulatory experts and MedTech executives on November 7 as they discuss the motivation behind seeking breakthrough designation, working with the FDA, and implications for development and commercialization. Don't miss out! #BreakthroughDevices #FDA #MedTech

📚 Digital Edition: Market Pathways January 2024 is now available • Market Pathways' editors highlight the major medtech policy issues and developments they'll be tracking in 2024 • Leaders of the public-private Medical Device Innovation Consortium (MDIC) discuss their current efforts to identify and address barriers to innovation throughout the medical device life cycle • And in Consultants Corner, Marina Daineko discusses the finer points involved in building risk-based biocompatibility plans. Get the edition here: https://bit.ly/3uJ1sPB #biocompatability #medicaldevices #medtechpolicy #medtech #medtechinnovation

Curious about the FDA Breakthrough Devices Program? Wondering if it's the right fit for your organization? Parexel's MedTech Regulatory Strategy and Health Advances MedTech consulting teams have researched the challenges and benefits of the Breakthrough designation and are excited to share their learnings with others in the #medicaldevices industry. Join our panel of regulatory experts and MedTech executives on November 7 as they discuss the motivation behind seeking breakthrough designation, working with the FDA, and implications for development and commercialization. Don't miss out! #BreakthroughDevices #FDA #MedTech

Exciting news in the medical device industry! The MDCG has just published the NB capacity dashboard which includes the results of surveys completed by NB over the past year. This is a great resource for anyone interested in understanding NB capacity in Europe. The European Commission’s Directorate-General for Health and Food Safety (DG SANTE) - through the European Health and Digital Executive Agency (HaDEA) - has commissioned a “Study supporting the monitoring of availability of medical devices on the EU market”. The study started in December 2022 and will be running for 36 months (December 2025). The study has been contracted to a consortium led by the Austrian National Public Health Institute (Gesundheit Österreich GmbH/GÖG), in collaboration with Areté and Civic Consulting. In the context of the study, a dashboard has been developed. The dashboard presents an overview of the data gathered from different stakeholders. In addition, comparable data from previous surveys of notified bodies conducted by the European Commission have been integrated in the dashboard. Check out the dashboard at the following link: https://lnkd.in/dFSUSAFt #MDCG #medicaldevice #NBcapacity #Europe

Curious about the Breakthrough Devices Program? Wondering if it's the right fit for your organization? Parexel’s MedTech Regulatory Strategy and Health Advances MedTech consulting teams have conducted research on the challenges and benefits of the designation and are excited to share those learnings with others in the medical device industry. Join our panel of regulatory experts and MedTech executives on November 7 as they discuss the motivation behind seeking breakthrough designation, working with the FDA, and implications for development and commercialization. Don't miss out! #BreakthroughDevices #FDA #MedTech

Curious about the Breakthrough Devices Program? Wondering if it's the right fit for your organization? Parexel’s MedTech Regulatory Strategy and Health Advances MedTech consulting teams have conducted research on the challenges and benefits of the designation and are excited to share those learnings with others in the medical device industry. Join our panel of regulatory experts and MedTech executives on November 7 as they discuss the motivation behind seeking breakthrough designation, working with the FDA, and implications for development and commercialization. Don't miss out! #BreakthroughDevices #FDA #MedTech

Curious about the Breakthrough Devices Program? Wondering if it's the right fit for your organization? Please mark your calendar now! Parexel’s MedTech #Regulatory Strategy and Health Advances MedTech consulting teams have conducted research on the challenges and benefits of the designation and are excited to share those learnings with others in the medical device industry. Join our panel of regulatory experts and MedTech executives on November 7 as they discuss the motivation behind seeking breakthrough designation, working with the FDA, and implications for development and commercialization. Don't miss out! #BreakthroughDevices #FDA #MedTech