MDR implementation can be a taxing and unsettling process. Learn what companies can do now to prepare for MDR, and what the new regulations mean broadly for the medical device industry.
Join us at OMTEC 2019 for a two-part EU MDR workshop. Part 1: Defining Sufficient Clinical Evidence for Your Device. Part 2: Top Challenges for Orthopedic Manufacturers.
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Citing evidence that patients may have an adverse biological response to certain types of metals, FDA announced that it is taking a closer look at materials used in medical devices, specifically metal-on-metal and nitinol.
Laser marking innovations are opening the door to more efficient, cost effective and easier to use technology for the last step of the long and complex manufacturing process.
A recap of three spine and three trauma products of interest that have gained FDA clearance since January. Devices include a spine cage from a traditionally biologics company, a foot/ankle device from a spine company, and additively-manufactured and computer assisted surgery products.
Lobo has been a member of the AdvaMed Board of Directors since 2012. The chairmanship uniquely positions Lobo to positively influence advances in the medtech industry.
Technology and talent could impact supply chain management departments in 2019. An industry veteran shares what you need to know to ensure that products are manufactured, packaged and delivered to your customers to spec and on time.
