Enabling Pharma Compliance with IVDR for Precision Medicine Trials

• How can pharma build IVDR capabilities to effectively deliver precision medicine trials in the EU?
• How to achieve IVDR compliance for trials with or without diagnostic company involvement?
• How to enable smooth collaboration between pharma, IVD manufacturer and/or CRO(s) for National Competent Authority submissions and approvals?

Speakers:

Aino Telaranta-Keerie

Senior Director, Global Precision Medicine Lead

Astellas Pharma