Christine Öberg joins SDS

We are proud to announce that Christine Öberg joins SDS as Regulatory Advisor in the Medical Device Development team.

Christine strengthens our multidisciplinary team by bringing her experience from product development of medical device and device for in vitro diagnostics, including software. Christine has strong knowledge of leading Risk Management activities and her experience from technical documentation, Quality Assurance and implementation of electronic document management system per ISO 13485 and 21 CFR Part 11 will fit SDS and our clients perfectly.