Couple of months back we thoroughly discussed about FDA’s expedited Regulatory pathways during medical emergencies. In that specific explanation as we listed the FDA’s tools and programs for expedited approvals with respect to review and approval of therapies, including biologics, this time we would like to bring the same perspective in relation to medical devices. Here we go with the US FDA’s perspective on registering, listing and importing medical devices that have been issued Emergency Use Authorization (EUA).
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