Develop regulatory submission strategies in agreement with defined product development objectives. Serve as the principal regulatory affairs liaison to FDA and other health authorities for assigned device projects. Prepare and submit device content for IND and NDA applications, or author 510K, and CE Mark regulatory filings.
https://www.indeed.com/viewjob?t=regulatory+affairs+manager&jk=94276ad24a06348c&_ga=2.111152845.832455782.1542907428-1408033885.1530798869
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