News

Quintiles' Real-World & Late Phase Research division leads AHRQ effort for evaluating patient outcomes since 2005.

A total of 81 medicines for human use were recommended for?marketing authorization by the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA), compared with 57 in 2012, according to EMA?s 2013 annual report.

The Pfizer-AstraZeneca courtship raises many fascinating questions about the future shape of the international pharmaceutical industry, but it is also revealing some remarkable displays of parochialism.

A total of 81 medicines for human use were recommended for?marketing authorization by the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA), compared with 57 in 2012, according to EMA?s 2013 annual report.

Product will serve as a data source for D360, supporting ongoing study monitoring and cross-study analyses

Medidata

Target Health and Life-On-Key have started the second year of a 2-year project grant.

The advent of Risk Based Monitoring will change the traditional Clinical Study Monitor’s (Monitor) role significantly.

Certara, a global technology-enabled drug development and drug safety consultancy, has launched its Pre-clinical Safety Store

Medidata Solutions announced that Sanofi has selected Medidata's targeted source document verification solution

NextDocs announced that leading pharmaceutical and biologics companies implemented late last year the NextDocs clinical solution suite

Groundbreaking site benchmarking data proves that sites with more staff certified are more profitable than those with fewer staff certified.

As of the April 2014 issue, the award-winning journal formerly known as The Monitor has been redesigned, rebranded, and reborn...

The ACRP announced it has changed the name of its official association journal

Top Pharma Increases Adoption of Medidata's Technology to Support Significant Operational Efficiencies Across Global R&D Organization

Company Integrates eTMF, CTMS and Investigator Portal to Bring Together Essential Clinical Trial Constituencies onto One Management System

New adaptive study designs, new target diseases, and global studies require on-demand packaging and labeling methods in order to keep operating costs under control.

Quintiles and Biogen Idec have entered a five-year collaboration that is intended to increase clinical trial efficiency.

Quintiles and Biogen Idec have entered into a five-year strategic clinical development agreement.

This year the AACR conference was focused on "Harnessing Breakthroughs, Targeting Cures."

In December 2013, Sanofi opened its submissions for the second challenge in its Partners in Patient Health

Logi Analytics announced that eClinical Insights has embedded its Logi Info into its core applications

The Society for Clinical Research Sites has launched its newest initiative, the Site Advocacy Group, with TransCelerate BioPharma as its SAG partner.

With all of the activity in CRO M&As the past three years, it?s slightly amazing that it continues...

Greenphire announced it has released new visual analytics functionality for its eClinicalGPS technology

Greenphire announced the release of new visual analytics functionality for its eClinicalGPS technology.

In November 2013, India's Drug Controller General required that all clinical trials must record on video a participant's informed consent.

Logi Info Embedded Into Core Applications to Help Advance Clinical Trial Research

Douglas Tsao, Vice President at Barclays, spoke on the outcomes of Merges & Acquisitions, and its impact on company stock prices.

MCC has just published an executive summary of its Risk Based Monitoring Usage Survey