1. Contact details{View data sources/studies associated with this centre}

Administrative Contact

Scientific Contact

2. Description

We share the vision to drive healthcare forward. To see how we can help accelerate progress and achievements. It’s bigger than better clinical trials. Or advances in technologies and analytics. Or faster insights. It’s about exploring a new path to better health outcomes via Human Data Science. Our global scientific, RWE and operational experts are developing innovative methods for RWE study design and execution combining secondary and primary data directly from patients and physicians. Applications include Post-authorization safety studies (PASS) Post-authorization effectiveness studies (PAES) Drug Utilization studies (DUS) Risk Evaluation and Mitigation Strategy (REMS) EU Risk Management Plan Pregnancy Registries Vaccine

3. Category

4. Available resources

5. Therapeutic/disease areas of research in drug safety/risk-benefit performed in the past 5 years

6. Design of drug safety/risk-benefit studies published in the past 5 years

7. Experience in collecting data directly from individual patients/respondents

Number of Studies

8. Access to data collection resources

9. Experience in secondary research and meta-analysis

10. Work with existing data resources in the past 3 years

11. Registries established by centre

12. Experience in collaboration in a study team

13. Current involvement in research networks

14. Interest in research opportunities which are funded

15. Interest in contract research only if free to publish results

16. Selected publications of the last 5 calendar years