Patients safety and the generation of high quality data are our first priorities
Centralized quality assurance
- Organizing, managing and updating SOP’s, WIS
- Provide relevant training of SOP’s and associated documents to sites
- Supporting quality control at the research sites to maintain consistent work flows in accordance with GCP, SOP’s and WIS
Local quality control
- Responsible for maintaining consistent day to day workflows in accordance with GCP, SOP’s and WIS
- Transforms into the generation of high quality data and securing patients safety and well-being during the entire study
Study initiation and study start-up
Our highly experienced central management team ensures shorter start-up timelines.
Our centralized Project Management provides visibility during all the steps of your clinical trial.