Date: 6 June, 2024
Location: UtrechtInc, Utrecht, The Netherlands
Introduction
If you're bringing a medical device or life science innovation to market, compliance with standards and regulations is crucial. In this session, the experts of Qserve guide you on navigating this complex landscape, including where to find regulations, what they mean for your company and device, and when to start with documentation.
Key topics covered during the workshop:
Regulatory, quality, and clinical affairs: understanding their implications.Essential information needed for product approval.Timing considerations for documentation commencement.This interactive session offers you the chance to ask questions and engage with fellow participants. Plus, following the workshop, you'll have the opportunity for one-on-one discussions with their experts to gain valuable insights and advice.
There is no need to register for the event. Drop by at UtrechtInc on June 6th at 10:00 CEST.
For more information about the event and UtrechtInc, please visit the website.
Qserve Attendees: