QP for devices in the EU: would you do this job?
This article was originally published in SRA
Executive Summary
The EU medtech sector is buzzing with activity when it comes to hiring experts to fulfil new roles in anticipation of the proposed new medtech regulations and the many added responsibilities they will bring. One critical new role will be that of the qualified person. Amanda Maxwell spoke with Arkan Zwick, regulatory affairs director at Croma Pharma, to find out what this role will involve.