
Parexel announced expanded services and capabilities in model-based drug development (MBDD) through its Quantitative Clinical Development (QCD) group.

Parexel announced expanded services and capabilities in model-based drug development (MBDD) through its Quantitative Clinical Development (QCD) group.


Certara®, a global biosimulation technology-enabled drug development company, announced the merger of its consulting group, Pharsight Consulting Services.

A case study by Pfizer & The Avoca Group on the development of an overarching strategy for Pfizer’s clinical trial quality metrics.


In response to increasing demand of Sharp Clinical Services.

goBalto, Inc., a provider of cloud-based clinical study startup solutions, announced its latest version of goBalto Activate.




Navitas, a regulatory service provider, announced that it has opened a new Latin America hub in Bogota, Colombia. Navitas' expansion into Latin America offers bilingual resources (Spanish and English) and provides document, report and submission level publishing for simple and complex submission applicatioms.


Quintiles and Quest Diagnostics announced the launch of Q2 Solutions, their new combined clinical trials laboratory services organization.


There is a lot of buzz about “the cloud.” Formally known as cloud computing, the cloud relies on sharing of Information Technology (IT) resources.


The Rethink Research Competition has opened voting for its People’s Choice Award.



The pilot involved several CDER employees working together with OEA employees to respond to drug related inquiries posted on FDA’s Facebook page.

BioClinica announced the opening of new and expanded offices in London and Munich.



A team of scientists at the University of Vermont has invented a new technique for discovering potentially dangerous drug interactions and unknown side-effects using Twitter hashtags.

A recent survey conducted by Applied Clinical Trials and SCORR Marketing on mHealth in Clinical Trials found the majority of respondents believe mHealth is only beginning its impact on our industry. To the question of challenges to implementing a mHealth strategy, clinical research professionals responded that having the knowledge to execute the skills was the leading challenge.

Acorn Regulatory, an ISO-certified medical device and pharmaceutical consulting firm, has customized programs to help U.S. manufacturers of drug-device combinations in meeting European regulatory approvals.


Medidata announced that its cloud-based technology platform has been adopted by JCR Pharmaceuticals Co., Ltd.
