In spring 2020, over 1,200 Changemakers will gather in Washington, DC to address critical health care issues at the 17th Annual World Health Care Congress at the Marriott Wardman Park.
Enhancing clinical training and education for professionals, not only aids HCP’s skills in ensuring proper tool use and the improvement of product awareness, but additionally the safety and overall care of patients. In today’s healthcare environment, doctors and hospitals look to bring about the best approaches for improved quality through cutting edge technology and new surgical equipment techniques, customizing care for the individual.
The U.S. Food and Drug Administration (FDA) is announcing the following public meeting entitled “Food and Drug Administration’s Communications About the Safety of Medical Devices.” The purpose of the meeting is to discuss the development, content and format of FDA safety communications about medical devices.
Anyone that has been a biopharma/medtech executive for more than 5 minutes knows that finding a forum of peers to have a deep, candid discussion about industry challenges is hard to find. Sure, there are conferences everywhere- but those are more about sponsor presentations and free keychains. Introducing LS2 – a private Summit designed by life science executives, like you.
Anyone that has been a biopharma/medtech executive for more than 5 minutes knows that finding a forum of peers to have a deep, candid discussion about industry challenges is hard […]
10x Medical Device Conference is the cross-functional event where the entire medical device ecosystem convenes to grow your skills, network, and profit. It’s designed to foster strong professional relationships among medical device players eager to learn smarter ways to do things with industry-leading resources.
Join us on April 23-24, 2020 for the 13th Annual Medical Devices and Diagnostics Statistical Issues Conference in Washington, DC. This annual conference brings together leading authorities from FDA, industry and academia to address the latest statistical trends and issues facing medtech organizations.
The Medical Device and IoT Summit explores all of these issues and more to provide actionable information for device manufacturers, software developers, provider organizations and investors.
Anyone that has been a biopharma/medtech executive for more than 5 minutes knows that finding a forum of peers to have a deep, candid discussion about industry challenges is hard to find. Sure, there are conferences everywhere- but those are more about sponsor presentations and free keychains. Introducing LS2 – a private Summit designed by life science executives, like you.
The In-Vitro Diagnostic Regulation (EU) 2017/746, which came into force in May 2017 with a transition period of five years, is intended to strengthen the current approval system for in-vitro diagnostics and makes substantial changes to the existing IVD Directive (98/79/EC) legislation.
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