Watch this webinar to:
What you'll learn
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
IVDR expertise
Hear Qualio's Kelly Stanton and Sumatha Kondabolu share tips and suggestions based on their extensive medical device quality management experience
Requirements breakdown
Take a deep dive into exactly what the IVDR demands and get to grips with how to unlock the European market
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