The search engine for healthcare databases
B.R.I.D.G.E. TO DATA® is Your Connection to Healthcare Databases Worldwide - a unique non-profit online reference describing population healthcare databases for use in epidemiology and health outcomes research. (NOTE: This site does not contain any proprietary data or actual datasets from any healthcare database.)
Drawing on decades of experience with databases, we developed this tool to allow users to identify key features and compare database profiles. This resource also serves as an educational tool for public health research and as a template for health systems planners to design or refine their healthcare data.
Access a specialized glossary
Contact our staff
Scan recent publications & administrative contacts for each database
Archive searches & create your own database collections
Search & Compare standardized profiles side-by-side
Access most up-to-date profiles verified by database managers
Identify population healthcare databases worldwide
Key Database Features
Types of databases include:
- Longitudinal EMR and claims
- Drug or disease specific cohorts
- National surveys
- National surveillance systems
- Spontaneous reporting systems
297 standardized database profiles
75 defined data fields
Profiles from 38 countries
What our customers say
This "database" of databases is very useful in my day-to-day activities as it allows me to find quickly which databases will fit the best regarding the research questions I have. It is very complete and contains information on countries for which it is sometimes difficult to find information elsewhere.
“I highly recommend researchers in the field of pharmacoepidemiology, pharmacoeconomics, and related disciplines to use B.R.I.D.G.E. TO DATA to identify a suitable database which will meet the needs of their research. Also pharmaceutical companies should look more often at the databases described by B.R.I.D.G.E. if they are required to conduct PASS studies.”
B.R.I.D.G.E. TO DATA is a tool which offers a shortcut between scientists and data for research. It allows the pharmaceutical community to gain time finding databases.
We are here at Booth #32 in Prague at the International Conference on Pharmacoepidemiology. Stop by for a demo and conduct your own search!
The Spanish Rare Diseases Patient Registry [Registro Nacional de Enfermedades Raras] is a registry of national scope which collects information on all persons diagnosed with any disease considered