27th & 28th November 2019, Brussels
Europe’s new legislative structure and narrow compliance time frames has increased emphasis of device and diagnostic quality professionals to rigorously update their quality management procedures to comply with new MDR and IVDR, while ensuring that continuous activities are not interrupted. Gaining practical insights of continuous audit readiness programs to ensure favourable results while managing continuing activities in both medical device and diagnostic sectors is of high concern, taking into account both European and international rules. The main areas of concern comprise of designing new strategies or the restructuring the existing processes of end-to-end supply chain activities, post-market surveillance and vigilance, collecting and managing increasing volumes of data from multiple sources, analysing opportunities of automating quality management processes to manage costs while preparing MDR & IVDR compliant products.
After successfully delivering tailor-made content in the inaugural edition of the conference, 2nd edition of the European Medical Device & Diagnostic Quality Assurance and Management Meeting will once again allow exchange of strategies and solutions through interactive session formats, real-world examples from peer experience as well as Notified Body representatives in this increasingly strict regulatory environment. This exclusive, two-day event will provide an unrivalled experience that will help inform and shape company strategy for the years ahead.
For more information about the conference speakers, please click here