Regulatory affair manager – medical devices
LausanneApproach People
...Drug (IND), New Drug Application (NDA), 510(k), Pre-Market Approval (PMA), or other regulatory filings, as required. Liaise with regulatory agencies, such as the FDA, EMA, or other regulatory authorities, to facilitate the review and approval process for new products or product changes. Provide regulatory guidance and support [...]
Category Management & Consulting
19 days ago in ApproachPeopleCOM