Icon-Structured-Authoring

The new Medical Device Regulations (MDR), which come into force by May 2020, include new features, new requirements and far more details than the old medical device directives. To understand the risks imposed on your business continuation, it is time to know the implications and start preparations on time. Iperion and Amplexor will help you with this, in a two-part webinar series. The second part starts on May 24th.

Professor Herman Pieterse, Professor in Clinical Pharmacology at the University of Ghent and Inti van Eck, Consultant at Iperion Life Sciences Consultancy, will explain what new MDR requirements mean for Clinical Trial setup and execution. They will provide you with valuable insights on how to best prepare and allow you to understand what you are required to do as a company to ensure compliance.

The webinar will address practical questions you might have concerning your Clinical Trials:

  1. Clinical Trials: what, where and when?
  2. Is my current trial setup sufficient to meet upcoming MDR requirements?
  3. How is my business impacted?

Register now for Part II Introduction to the MDR, starting May 24

Contact us for more information +31 73 648  8000 or send an email to webinars@iperion.nl