European MDR Compliance Modular Workshop-Training program 2017

The new MDR will affect all Medical Device manufacturers. Scope & Plan, GAP assessment, Portfolio analysis, Global Impact Assessment are just some of the steps on the road to MDR implementation that must be addressed to ensure compliance.


Post date: March 01, 2017
Subscribe to the Qserve Newsletter and follow us on LinkedIn
Want more information? Please contact us.
Information request