Regulatory Affairs Talent in the Greater Philadelphia Region

20 years

BS

510(k), IDE, PMA, CE marks, and global product registration. Industry: Medical Device

20 years

BS

Submission management, CMC collaboration, labeling management, project management, and development of tracking tools. Industry: Pharmaceutical

20 years

MS

CMC submission/review, eCTD, and IND/NDA submission review. Industry: Pharmaceutical

19 years

BS

510(k), MDR submissions, and labeling review. Industry: Medical Device

12 years

BS

Controlled document tracking, submission coordination, IND, annual reports, and PSURs. Industry: Pharmaceutical

7 years

BS

Labeling review, ANDA filing, and eCTD. Industries: Pharmaceutical, Medical Device

6 years

BA

Proofreading labeling artwork, inserts, and Veeva Vault. Industry: Pharmaceutical

6 years

BS

Global product registration, eCTD, and document management. Industry: Pharmaceutical, Medical Device