2018 MedTech Events: FDA Submissions, Cybersecurity, Recalls and More
From learning how to plan for FDA submissions to real-world tools to manage risk to addressing critical cybersecurity challenges, MedTech Intelligence has several practical workshops and conferences for the first half of 2018. The year kicks off with a virtual workshop series on FDA submissions —510(k) and de Novo pathways to market, PMA submissions, and FDA submissions strategy. Register for any of the three workshops here.
Think statistics are scary? Fear not. In February, MTI has a virtual course designed for non-statisticians (and no prior statistical training is required) about how to use statistical methods in medical device development, testing manufacturing and postmarket surveillance. Register for the virtual event, taking place February 13–14 here.
Other conferences include Cybersecurity Vulnerability Management and Cybersecurity Patch Management and the sixth annual Medical Device Recalls program (May 14–15). The full list is available on MedTech Intelligence’s Events & Webinars page.
Related Articles
-
As of June 1, 2022, the Center for Devices and Radiological Health plans to accept all non-COVID in vitro diagnostic (IVD) pre-submissions.
-
Manufacturers preparing premarket submissions should provide performance specifications for the quantitative imaging functions, supporting performance data, and sufficient information for the end user to obtain, understand and interpret the values provided.
-
With the ever-increasing adoption of connected devices, the agency is emphasizing the need for effective cybersecurity.
-
As VP of Product Marketing for a MedTech startup, my role is to champion pioneering medical technology, strategically spark interest and drive it out of the design lab and into the field where it will ultimately change, or even save…
