Medical Device RA Submissions
Medical Device Regulatory Affairs Submissions
Our client is currently in need of a consultant to come on board and help their submissions team. Right now, they are looking for someone who can come on site who is well versed in active medical devices. This person will be working on 510k’ s around devices with software and electrical components.
Day to Day Responsibilities:
This consultant will be responsible for 510k submissions around active medical devices. Right now, the client does not have anyone on site who is well versed in the regulations surrounding devices with software and electrical components and needs someone to guide them through the submission process. This consultant will be expected to be very hands on as they will be working directly with the submission process.
Active Medical Devices