
FDA hands down beats other regulatory authorities in approving oncology drugs.

Future growth could be impacted by a marked skills shortage, according to a survey from Berkley Group.

Thomson Reuters Cortellis Competitive Intelligence

ACRES has unveiled a scheme to create an integrated information-management platform designed to support clinical research worldwide.

Finding the right CTMS is a long, difficult process.

Concerns are emerging among researchers that the European Medicines Agency is not following through with its pledge to open clinical trials data to public scrutiny.

Medidata announced that it is partnering with TransCelerate BioPharma

EMA's crowning achievement in transparency?proactive release of clinical trials data?is only weeks from finalization.

As confidence returns to job seekers, high levels of staff movement could impact on organizations' growth.

Collaboration to explore key components of recommended Risk-Based Monitoring methodology

A major initiative to create an integrated information-management platform supporting clinical research worldwide was announced today.

ECRIN is encouraging all clinical researchers to get involved in International Clinical Trials' Day.

PAREXEL announced the launch of its Perceptive MyTrials Data-Driven Monitoring solution.

For any Brit involved in medical publishing, The BMJ is the holy grail.

Cloud-based Platform Automates and Streamlines Clinical Trials Process, Saves Innovative Biotech Valuable Time and Resources

Biopharmaceutical company Versartis, Inc. has selected Comprehend Systems

In early May, Bloomberg news reported the FDA will be conducting studies into generic extended release Toprol XL after almost 3,500 adverse incident reports have amassed since March 2009.

Abstracts related to the conduct of clinical trials, not the actual trials results, from ASCO can be found under the category Health Services Research.

Covance announced it has acquired Medaxial.

Expanding global market access, reimbursement, and communications solutions.

Draft terms of reference and membership of panel now on bmj.com

This month, let's look at a quality metric that's useful for tracking both protocol and site performance: subject retention percentage.

Amidst all the talk about reducing the time and scope of clinical trials to accelerate drug testing and approval, medical product development still requires researchers and regulators to "get the right answer".

ICON announced that Aptiv Solutions, an ICON company for the design and implementation of adaptive trials, has released ADDPLAN DF 3.0

ICON plc, announced Aptiv Solutions, an ICON plc company leading the design and implementation of adaptive trials, has released ADDPLAN DF 3.0

PRA announced the addition of capabilities and services to its Lenexa, KS location.

Immunochemistry Services Now Available in Kansas

Thomas Verish, Group Director of Data Operations Services at Bristol-Myers Squibb, elaborated on their risk-based monitoring pilot.

Most business leaders acknowledge the pitfalls of organizational silos: they breed inefficiency and signal systemic malfunctioning.
