The centralized project management service provides our sponsors and their delegates effortless access to study related information collectively from all study sites involved
- Updated reports at agreed time intervals
- Supporting submission and implementation of amendments
- Collecting documents needed for submission
- Additional study specific training
- ICF implementation
- Other study related query resolutions
- A structured escalation process with the flexibility to adjust to specific sponsor requests
Our centralized Project Management provides visibility during all the steps of your clinical trial
Study initiation and study start-up
Our highly experienced central management team ensures shorter start-up timelines.
Our experienced research team combined with harmonized workflows guarantees the generation of consistent high quality data.