Medical Device Regulation

EWMA has taken the initiative to explore the possibilities for a joint dialogue (led by industry and health care professionals) with the regulatory authorities concerning the MDR-related challenges and opportunities defined by wound care health professionals and the industry. In light of the far-reaching consequences that the MDR changes may prompt in terms of optimal patient care, we have invited regulatory experts to host a workshop, covering the challenges and opportunities related to the new medical device regulations.

If you are interested in learning more about the ongoing transition from previous directives to MDR and discussing the related challenges and opportunities for the industry and health care professionals, you should attend the EWMA-hosted workshop on the topic.

Presentations and Q&A's with

Edwin den Braber, PhD

Managing Partner, GR Consulting LLC

Bernhard Weber

Associate Director Quality Management & Regulatory Affairs Healthcare products at Diapharm GmbH & Co. KG

Marcia Nusgart

Executive Director, Alliance of Wound Care Stakeholders (US)