We're excited that Kirsten Sander, from Aurevia GmbH, will be speaking at the Medizinprodukte für Einsteiger*innen seminar hosted by FORUM Institut on 20-21 October.
This online seminar is hosted by FORUM Institut and provides a practical introduction to the medical device lifecycle under MDR and MPDG, covering topics such as clinical evaluation, clinical investigations, conformity assessment, vigilance and post-market surveillance. A great opportunity for professionals looking to build a solid foundation in medical device regulation. Learn more and register.
At Aurevia, we support life science companies throughout the product lifecycle with expertise in quality assurance, regulatory affairs, and clinical research. Whether you're navigating regulatory requirements, strengthening your quality management system, or planning clinical activities, our experts help you move forward with confidence. Contact us.
