MDTmag.com guest blog: 7 Tips for Painless FDA 510(k) Regulatory Submissions
November 14, 2013
7 Tips for Painless FDA 510(k) Regulatory Submissions, a guest blog in MDTmag.com by Vincent Crabtree, Ph.D., Regulatory Advisor and Project Manager, StarFish Medical, offers advice and examples for navigating the FDA Regulatory Clearance using the 510(k) Pre-market Notification process. A well planned submission from an early stage containing all the necessary information is a good way to set an FDA reviewer at ease.
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