IVDR compliance: tips and best practice

Watch this webinar to:

  • Learn about the key requirements of the EU's In Vitro Diagnostic Regulation (IVDR) as it comes into effect

  • Understand the key actions your business needs to take for full compliance

  • Access compliance tips and tricks for a smoother, stress-free CE marking journey


What you'll learn

  1. IVDR expertise
    Hear Qualio's Kelly Stanton and Sumatha Kondabolu share tips and suggestions based on their extensive medical device quality management experience

  2. Requirements breakdown
    Take a deep dive into exactly what the IVDR demands and get to grips with how to unlock the European market

  3. Actionable compliance pathway
    Learn what your business needs to do to get your product CE marked and approved under the IVDR - and how you should start your compliance journey