|The FDA announced a brand new docket and a “comment period” regarding refurbishing, reconditioning and remanufacturing medical devices. Anyone responsible for servicing, repairing and selling these medical devices/parts needs to be aware of this very important announcement.
This 60-minute webinar will feature an Expert Panel from all segments of the industry (hospital technicians/engineers, ISO’s, third party parts/equipment providers, Associations, etc.) to help inform you of what your next steps should be.
You can submit your question for our Expert Panel by emailing firstname.lastname@example.org. Questions will be accepted during the live webinar, as well.
Deadline for FDA comments is May 3rd, 2016, so you don’t want to miss this highly valuable and informational meeting!