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Every patient counts

Better organized patient communities attract more research interest - and treatments.

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Empower patients & researchers

Patients can speed research by sharing their medical history and testing results with researchers. 

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Share data with researchers

Interested researchers can register to gain access to de-identified patient data and tools.

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Identify clinical study candidates

Speed treatments to market by identifying pre-validated clinical study candidates.

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M.A.P. Project Featured in WSJ

PatientCrossroads collects detailed breast cancer survivor data for the Cancer Support Community M.A.P. Project.

Read the Wall Street Journal article  

 

Download the full report to see how you can harness the power of your community with PatientCrossroads.


 

Integrated Registry & Repository Services

Integrated Disease Registry and Repository Services through PatientCrossroads and the NIGMS Repository at Coriell

 

Patient advocacy organizations and research investigators can now take advantage of a new integrated registry and repository resource to further advance rare disease research.

Learn More

Office of Rare Diseases Research GRDR

The Office of Rare Diseases Research (ORDR) in collaboration with PatientCrossroads, Children Hospital of Philadelphia and WebMD, has launched a pilot program to establish a Global Rare Diseases (Patient) Registry and Data Repository (GRDR) to collect patient clinical information without any personal identifiers (de-identified information), for clinical research.

Learn More

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