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News

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eShowcase: Clintrace 4.1

Applied Clinical Trials

Release takes adverse event reporting to a new level, complies with FDA's new rules

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Applied Clinical Trials

Document management suite gets training records tool with eCTD capabilities slated for V4.0

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Reflections

Applied Clinical Trials

What has the industry and the FDA accomplished this year and what still needs to be done?

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Clinical Lab Directory

Applied Clinical Trials

A listing of clinical laboratories arranged alphabetically, with addresses and contact details.

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eShowcase: LabPas CT 2.5

Applied Clinical Trials

Phase I package adds formulary accountability, recruitment, lab, and EDC features

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eShowcase: LabPas CT 2.5

Applied Clinical Trials

Phase I package adds formulary accountability, recruitment, lab, and EDC features

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Applied Clinical Trials

Regulatory submission solution addresses the needs of smaller biotech and pharma companies

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eShowcase: LabPas CT 2.5

Applied Clinical Trials

Phase I package adds formulary accountability, recruitment, lab, and EDC features

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Applied Clinical Trials

System enables IRB members to review ?s in near real-time from anywhere in the world

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Clinical Lab Directory

Applied Clinical Trials

A listing of clinical laboratories arranged alphabetically, with addresses and contact details.

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Applied Clinical Trials

What do the G8 Summit, national security, and the pharmaceutical industry have in common?

Applied Clinical Trials

Allied Research International (ARI), Canada's leading contract research organization (CRO), announced today that it has acquired key assets of South Florida Bioavailability Clinic International's (SFBC) Miami, Florida operations.

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eShowcase

Applied Clinical Trials

Tools for Clinical Trials Professionals

Phase Forward Incorporated (NASDAQ: PFWD), a leading provider of data management solutions for clinical trials and drug safety, today announced its financial results for the second quarter of 2006.

Applied Clinical Trials

Shire plc announced today that it has submitted a new drug application (NDA) to the U.S. Food and Drug Administration (FDA) for SPD465, an investigational amphetamine compound for the treatment of Attention-Deficit/Hyperactivity Disorder (ADHD) in the adult population.

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eShowcase

Applied Clinical Trials

Tools for Clinical Trials Professionals