More Clinical Articles

Clinical

Guest Feature - Guidelines for Optimizing Your Time-to-Market

Editor, (Apr 16, 2007)

Pharmaceutical companies have invested heavily in speeding the technical aspects of new drug development.
Commercial

Is pharma R&D productivity turning the corner?

Editor, (May 16, 2006)

According to new research from the Tufts Center for the Study of Drug Development (CSDD), pharma’s R&D pipeline may be in the beginning of a rebound.
Clinical

Pharma R&D productivity poised to improve, study says

Editor, (Jan 26, 2006)

The willingness of drug developers to use new discovery tools, such as pharmacogenomics, and the aggressive management of clinical trials, through advanced data analysis and outsourcing to lower cost
Clinical

Guest Opinion: Clinical Trial Data Management Outsourcing in India

Editor, (Jun 28, 2005)

India has developed into a super power for IT skills and has become a major hub for pharmaceutical and biotech manufacturing And contract research, the outsourcing business in various other segments
Clinical

Kendle International to Implement Logos Technologies ALPHADAS clinical trial solutions

Editor, (Dec 22, 2004)

The solutions are designed to help Kendle streamline its existing clinical data processes and are expected to provide significant cost savings.
Clinical

INC Research and IntraLinks form strategic relationship to Streamline Clinical Trials

Editor, (Oct 28, 2004)

INC Research will use IntraLinks’ 21 CFR part 11 compliant digital workspaces to accelerate secure information exchange during critical start-up and conduct phases of clinical trials, and to ma
Clinical

Sankyo Pharma uses IntraLinks for clinical trial communications

Editor, (Oct 12, 2004)

This study will involve 22 countries and about 220 centres throughout Western and Eastern Europe, and will recruit more than 4,400 patients.
Commercial

invivodata urges the FDA to address patient reported outcomes data in its Critical Path Initiative

Editor, (Oct 12, 2004)

The FDA's Critical Path initiative aims to streamline the new-drug and medical-device development and approval process, allowing effective new products to get to market faster while keeping costs
Clinical

GSK standardizes on Phase Forward's Inform EDC solution

Editor, (Aug 24, 2004)

Already a customer of Phase Forward's Clintrial clinical data management solution (CDMS), GSK will deploy InForm and Phase Forward consulting and support services across its Phase I-IV clinical tr
Clinical

Eli Lilly to report results of trials via registry

Editor, (Aug 10, 2004)

The move comes amid criticism drug companies may hide negative results of clinical trials of their drugs and follows a lawsuit by New York Attorney General Eliot Spitzer against rival GlaxoSmithKline.

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