Precision Medicine Strategic Considerations for Global Market Access: From Early CDx Development to Clinical Trials & Overcoming Regulatory Hurdles
Time: 8:30 am
day: Conference Day 1 AM
Details:
- Understanding regulatory considerations for USA, EU and APAC to expedite approvals
- Creating a robust CDx strategy to expedite from clinical trials through to CDx launch
- Key considerations for diagnostic tests in clinical trials and using this data for global submissions
