By Jon Speer, in Quality Management System (QMS) and EU MDR and Medical Device Quality Management System How prepared is your quality management system for the new requirements of EU MDR for medical devices that will go into effect in less than a year? The European …
Keep ReadingThe Essential Guide to Preparing Your QMS for EU MDR
By Doug Beveridge, Principal and Health Care Practice Leader at The Alexander Group This is an exciting time for health care. MedTech companies are expanding beyond traditional products and boundaries. Value is moving from a physical product to the information …
The Real World Evidence panel at The MedTech Conference will feature representation from the FDA, NEST and other industry representatives. Below, moderator Seth Goldenberg (vice president of medical devices and diagnostics at Veeva) and panelist Manish Bharara (senior manager of …
Keep ReadingReal-World Evidence: The need for continued dialogue across device stakeholders.
By Kolaleh Eskandanian, Ph.D., MBA, PMP, vice president and chief innovation officer at Children’s National Health System Are you interested in advancing device clinical trials in general, but also learning about potential innovative pathways for pediatrics? If yes, then make …
By Chris Rao, Director, Alira Health Clinical Planning a relevant and accurate budget, regardless of the trial phase or indication, can be one of the most challenging aspects of the clinical trial process. Though it is one of the most …
Keep ReadingFour Critical Factors for Clinical Trial Budget Success
by Khatereh Calleja, J.D., President and CEO of Healthcare Supply Chain Association (HSCA). As the health care landscape continues to evolve, fostering the development and implementation of cutting-edge technologies in the health care system is more important than ever before. …
Keep ReadingIntroducing Innovation into the Health Care Supply Chain
We spoke with Pat Schafer, Managing Director at Grant Thornton, to learn about his experience as a 2018 conference sponsor. Hear what Pat has to say on the benefits of sponsorship, the types of companies he was able to meet …
By Matt Singer, ZS Principal In a recent ZS survey with hospital executives in the U.S. and Europe, we found that 90% of respondents think that medtech manufacturers can’t succeed with product innovation alone. Moreover, that same number of respondents …
Keep ReadingA Modern Approach to Portfolio Strategy: From Feature Innovation to Value Innovation
By Nancy Travis, Vice President, International Compliance and Governance at AdvaMed At the Global MedTech Compliance Conference that occurred in Paris this past May, I heard a lot of discussion around values-based compliance systems. This to me is emblematic of …
We caught up with Craig Ackerman of the Alexander Group to learn about his experience as a 2018 conference sponsor. Hear Craig’s perspective on the benefits of sponsorship, the types of companies he was able to meet onsite and the …
