Daphne King

Company: BioMarin Pharmaceutical

Job title: Associate Director, Regulatory CMC

Seminars:

Development of a Device with EU MDR in Mind 9:30 am

Incorporation of GSPR – Annex 1 compliance from device conception onwards, to increase device design process efficiency and decrease development timelines Clinical Evaluation – Article 61, Annex XIV Part A – considerations for fast progression through regulatory process Development of a Regulatory Strategy Compliant with Article 10, Annex IX and how this will assist your…Read more

day: Conference Day Two