FDA's Medical Device Software Regulation Strategy
from ReferralThis seminar will focus on addressing these concerns and educating participants on FDA’s recent medical device software regulation strategies.
Seminar instructor Casper Uldriks is an ex-FDA official who has spent 32 years with the FDA. His engagements focus on advertising and promotion, recalls, corrections and removals and enforcement. He currently trains FDA personnel and counsels clients on wide range of topics, including: FDA inspections; import operations; advertising and promotion; corrective and preventive actions; medical device reporting and corporate reorganization to improve conformance to FDA’s requirements.
DOWNLOAD BROCHURE
The medical device trade and healthcare professionals remain plagued by other issues, such as the interoperability of devices from different manufacturers, or software validation that is limited to the immediate use of the software rather than its performance with other software programs, and software hacking protection applications. In case of software malfunction, fixing the malfunction or bug can get more difficult as software gets increasingly sophisticated, customized by users and placed in a network system. Under these circumstances, it is difficult to decide who is responsible for managing and fixing software problems. (from )
-
This event has passed.
Through March 1, 2019February 28, 2019 to March 1, 2019 -
San Francisco, CA
, , -
Contact Ashutos Swain for more information
8887172436 or [email protected] -
This listing has not been linked to an event on Facebook.
Suggest a Facebook event for this listing
Directions are calculated based on the address provided by the event submitter and may not be precise. Please contact the event coordinator for more detailed information.