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Biomarker Data Repository

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Multiple Sclerosis Outcome Assessments Consortium

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Critical Path for Alpha-1 Antitrypsin Deficiency

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Patient-Reported Outcome Consortium

CPAD

Critical Path For Alzheimer’s Disease

PKDOC

Polycystic Kidney Disease Outcomes Consortium

CPP

Critical Path for Parkinson’s

PredicTox KE

PredicTox Knowledge Environment

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Critical Path for Rare Neurodegenerative Diseases

PSTC

Predictive Safety Testing Consortium

CP-SCD

Critical Path for Sickle Cell Disease

QuantMed

Quantitative Medicine Program

CPTA

Critical Path to Therapeutics for the Ataxias

RDCA-DAP

Rare Disease Cures Accelerator-Data and Analytics Platform

CDRC

CURE Drug Repurposing Collaboratory

RD-COA Consortium

Rare Disease Clinical Outcome Assessment Consortium

DCC

Data Collaboration Center

TB-PACTS

TB-Platform for Aggregation of Clinical TB Studies

D-RSC

Duchenne Regulatory Science Consortium

TTC

Transplant Therapeutics Consortium

eCOA Consortium

Electronic Clinical Outcome Assessment Consortium

TOMI-T1D

Trial Outcome Markers Initiative in T1D Consortium

FA-ICD

Friedreich’s Ataxia Integrated Clinical Database

TRxA

Translational Therapeutics Accelerator

HD-RSC

Huntington’s Disease Regulatory Science Consortium

T1D

Type 1 Diabetes Consortium

INC

International Neonatal Consortium

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CFAST

Coalition for Accelerating Standards & Therapies

PTC

Pediatric Trials Consortium

CPTR

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Home>News & Events>July 10, 2013

News

July 10, 2013 PRINT PDF

July 10, 2013

FDA and EMA Reach Landmark Decisions on Critical Path Institute’s Clinical Trial Simulation Tool for Alzheimer’s Disease

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