This course focuses on gathering and using clinical evidence for CE marking and post-market compliance, aligned with the new MDR. We offer customized ..
training solutions for technical, commercial, and personal development needs. Specifically designed for individuals involved in gathering clinical evidence for medical devices, this intensive course covers all activities related to pre- and post-market studies. It also provides information on European regulations for clinical evidence gathering and medical device studies. Participants will receive practical advice from industry experts on conducting studies in Europe and collecting clinical data to comply with the new MDR. The online format allows for clear visibility of the speaker and presentation. Janette is a highly knowledgeable and well-prepared speaker who provided extensive content and information throughout the two days.