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March 2, 2013

Opportunities and Challenges of Safety Biomarker Qualification: Perspectives from the Predictive Safety Testing Consortium

March 1, 2013

The Patient-Reported Outcome (PRO) Consortium at the Critical Path Institute (C-Path)

March 1, 2013

Critical Path Institute’s Electronic Patient-Reported Outcome Consortium

March 1, 2013

The advantages of frontotemporal degeneration drug development (Part 2 of frontotemporal degeneration: the next therapeutic frontier)

March 1, 2013

Global standardization measurement of cerebral spinal fluid for Alzheimer’s disease: an update from the Alzheimer’s Association Global Biomarkers Consortium

February 21, 2013

Critical Path Institute Names Martha Brumfield CEO

The Board of Directors of the Critical Path Institute (C-Path) announced today that Martha Brumfield, Ph.D., has been named interi

January 30, 2013

CFAST Announces Parkinson’s Disease Drug Development Milestone: Release and Availability of a PD Therapeutic Area Data Standard

January 12, 2013

Patient-Reported Outcomes In Clinical Trials Of CKD-Related Therapies: Report Of A Symposium Sponsored By The National Kidney Foundation And The US Food And Drug Administration

January 8, 2013

Understanding Placebo Responses In Alzheimer’s Disease Clinical Trials From The Literature Meta-data And CAMD Database

January 6, 2013

ePRO Systems Validation: Clearly Defining The Roles Of Clinical Trial Teams And ePRO System Providers

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