News

Veeva Systems introduces innovations to its Veeva Vault product for regulated content management for life sciences.

The integration of Chesapeake IRB and IRB Services is now complete.

Veeva Vault balances global harmonization with local autonomy for regions, departments, therapeutic areas

Cloud-based platform integrates operations in the United States and Canada.

US researchers and regulators continue to support the use of randomized clinical trials to test potential treatments and vaccines to combat the Ebola virus...

The most advanced IRT user interface available.

YPrime, LLC released its latest addition to the YPrime clinical research software suite.

I recently visited the Caribbean isles, and on my way at the airport, I noticed prominent CDC disclaimers about an equatorial viral disease: Chikungunya.

Cot? Orphan's new Clinical Research Organization fortifies its foundation as a full-service industry leader in orphan drug regulatory affairs and development.

Medidata announced positive results of a data-driven analysis conducted in collaboration with TransCelerate BioPharma

Cot? Orphan announced it will now provide CRO services that will help organizations navigate the clinical trials process

CTI announced that is has opened an office in Geel, Belgium.

New product aims to give CROs and sponsors a competitive advantage

CTI has opened an office in Geel, Belgium

Cost to Develop and Win Marketing Approval for a New Drug Is $2.6 Billion, According to the Tufts Center for the Study of Drug Development

Cost to Develop and Win Marketing Approval for a New Drug Is $2.6 Billion, According to the Tufts Center for the Study of Drug Development

goBalto announced the release of Analyze

In this article, the authors discuss patient-centered research (also termed "direct-to-patient") that uses the "remote" study approach.

Joint Initiative Evaluates Impact of mHealth and Cloud-Based Technologies on Patient Engagement, Data Quality and Operational Efficiencies in Clinical Trials

Medidata announced the completion of a method development project conducted in partnership with GlaxoSmithKline plc

My recent blog has been overtaken by history, with the departure of Guido Rasi from his post of Executive Director of the European Medicines Agency

Debuting at CNS Summit 2014

Celgene Corporation uses the PHT Corporation SitePad System and StudyWorks to collect patient-driven eData for OTEZLA (apremilast) tablets approved by the FDA in March 2014

Bracket announced the release of Rater Station 3.5

ActiGraph has announced the release of the ActiGraph GT9X Link activity monitor.

Technology Provides Access to Patients Living Far from Study Site

SGS Life Science Services announced that its Biometrics group became a Medidata Rave accredited partner.

SGS Life Science Services announced that its Biometrics group became a Medidata Rave accredited partner.