CROs/Service Providers

Icon, Carnegie Mellon partner to research ways to improve study patients’ understanding of Informed Consent

Monday, March 30, 2015 08:00 AM

By Ronald Rosenberg
CenterWatch Staff Writer

Ongoing concerns about clinical trial participants’ lack of understanding of the Informed Consent process has prompted Icon to sponsor a series of research projects at Carnegie Mellon University (CMU) to find better ways to improve comprehension, including the use of multimedia tools and advances in behav­ioral decision research.

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PPD first to migrate data to the Oracle Health Sciences Cloud

Thursday, March 26, 2015 02:58 PM

PPD is the first company to migrate trials from an on-site installation of Oracle Health Sciences’ Siebel Clinical Trial Management System to Siebel Clinical Trial Management System Cloud Service—creating a highly available, centralized trial database that lowers costs, simplifies management, improves the accuracy of multi-CRO clinical trial data and accelerates studies.

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Parexel to acquire Quantum Solutions India

Thursday, March 26, 2015 02:56 PM

Parexel International, a Boston-based global CRO, has signed a definitive agreement to acquire all of the business assets of privately-owned Quantum Solutions India (QSI), a provider of specialized pharmacovigilance services.

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Recipharm, Adroit Science collaborate to expand service offering

Thursday, March 26, 2015 02:51 PM

Two Swedish companies, Recipharm, a contract development and manufacturing organization (CDMO), and Adroit Science, a provider of laboratory and consultancy services, have formed a new strategic collaboration.

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BioClinica opens North Carolina office

Wednesday, March 25, 2015 02:56 PM

BioClinica has opened a Research Triangle Park (RTP) office in North Carolina in response to a rapidly expanding customer base of study sponsors and CROs with whom it has strategic partnerships.

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Paidion Research, a new pediatric CRO, launches

Wednesday, March 25, 2015 02:48 PM

Paidion Research, a new CRO focused exclusively on pediatrics and specializing in NICU and PICU populations (neonatal and pediatric intensive care), recently opened for business. Headquartered in Durham, N.C., Paidion combines pediatric clinical pharmacology experience with innovative pediatric regulatory strategies and trial methodologies to provide best-in-class service to drug and device development partners in industry, government, academia and nonprofits.

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Catalent launches Quality, Product Development & Regulatory Affairs organization

Thursday, March 19, 2015 02:55 PM

Catalent Pharma Solutions, a Somerset, N.J.-based global provider of advanced delivery technologies and development solutions for drugs, biologics and consumer health products, has formed the Quality, Product Development & Regulatory Affairs organization, established to build upon Catalent’s experience in new product development, regulatory excellence, reliable supply and quality. Sharon Johnson, senior vice president, global quality & regulatory affairs, will head up Catalent’s new organization.

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Study: Merit increase budgets continue to rise in the global CRO industry

Thursday, March 19, 2015 12:11 PM

Merit increase budgets continue to rise in the global CRO industry, according to a study conducted by HR+Survey Solutions. The survey found the overall global (all countries combined) average budgeted salary increase for 2015 is 4.14%, up from 3.94% in 2014, and significantly higher than the overall average actual increase in 2014 of 3.7%.

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Patheon to acquire IRIX Pharmaceuticals

Wednesday, March 18, 2015 01:26 PM

Patheon will acquire IRIX Pharmaceuticals of Florence, S.C., which specializes in difficult to manufacture Active Pharmaceutical Ingredient (API) needs for drugs from early and late development through commercial launch. Patheon expects to close the transaction in the next 60 days.

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ACRO holds initial meeting of CRO Forum

Wednesday, March 18, 2015 01:21 PM

The Association of Clinical Research Organizations (ACRO) has held the inaugural meeting of the CRO Forum in Washington, D.C. The Forum was established last October as the primary vehicle for interaction between the CRO industry and TransCelerate BioPharma.

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July 27

AB Science warned about putting study volunteers in danger

FDA, Google unite to detect search-data adverse events

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The CenterWatch Monthly


Integrated research partnerships build momentum
Research function provides infrastructure, leverages large pool of health systems' patients and data

'Right to Try' laws challenge clinical trial process
20 states pass, 20 more pending allowing access to study drugs without FDA and IRB approval

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TransCelerate Biopharma turns three
High-profile consortium has made inroads fixing wasteful practices, but it still has more work ahead

Pharma industry improves its tarnished reputation
Delivering innovation, social responsibility will help rebuild trust

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