Medical Device Manufacturer, seeking a Regulatory Affairs professional to help us create and submit a Traditional 510(k) Pre-Market Notification package. Please contact us for further information.
8 freelanceria on tarjonnut keskimäärin %project_bid_stats_avg_sub_26% %project_currencyDetails_sign_sub_27% tähän työhön
More than 4 years experience in RA area, medical devices and drugs submissions. Relevant Skills and Experience RA submissions, medical devices and drugs submissions