Main tasks in the project
- In WP1, Takeda will act as the Industry co-lead and assist with consortium management activities.
- In WP2, Takeda will contribute to the design of the study protocols and assist with the statistical data analysis.
- In WP3, Takeda will support the device selection process.
- In WP6, Takeda will contribute their expertise in devising the operational and monitoring strategies of the clinical validation study and advise on the associated regulatory issues.
- In WP7, Takeda will provide data