Specialisms / Regulatory Affairs
The new Rockstars
In the last 10 years, companies have invested more and more in Regulatory Affairs, both in PMA and PMS areas. With MDR and IVDR looming, and a lack of graduates coming into the space, opportunities are rife.
Due to the increasing complexity of the role, regulatory positions are becoming more defined. If you have RA experience with high-risk devices, rest assured you can build yourself a great career.
Vado Med Tech have in-depth knowledge of this key function and typically have opportunities in the following areas:
PMA • PMS • Global submission and registrations • Vigilance • 510k • CE Marking • IDE • Risk Management • Compilation and review of technical documentation • Notified Body Liaison • Consulting • Labelling • Promotional Material.