Impact of EU/UK IVD Regulatory Changes on Precision Medicine Development for the Pharmaceutical Industry
Time: 11:15 am
day: Day One Morning
• How will the incoming EU and UK regulatory changes for IVDs and CDx impact precision medicine development?
• How will the UK will be aligned with Global and EU IVD and CDx Regulations?
• How will these changes be implemented and who is going to pay for them?
• How can internal pharma R&D and commercial teams prepare for compliance with these new regulatory changes?