CRF Health, a leading global provider of ePRO solutions for the Life Sciences Industry, announced that John Harrison, PhD, had accepted an appointment as Scientific Consultant. in this role, John will provide expert advice on both patient and clinician reported outcomes in Central Nervous System (CNS) related clinical studies.

John has over 15 years of extensive experience in selection and integration of cognitive testing into drug development programs. Most recently he was Principal Scientist at CogState Ltd, a company providing cognitive testing services to pharmaceutical companies. He is also Honorary Senior Lecturer at Imperial College in London where, among other topics, he invested cognitive change as a function of disease progression in Alzheimer's disease and HIV infection. Prior to his position with CogState, John was an independent consultant to drug development companies thought CPC Pharma Services, a consultancy that services pharmaceutical and biotechnology companies.

John's education includes a BSc in Psychology from the University of Hertfordshire and a PhD in Neuroscience from the University of London. He is currently studying for a BA in Classical Studies from the Open University. He resides in the West of England with his wife Rachel and two children. In addition to his interest on the measurement of cognitive change, he enjoys ballet, opera, and studying classical civilization.

Rachael King, CEO, commented, "we are very please to have recruited Dr. Harrison in a consulting role. The world-wide aging population has triggered growing interest in Dementia and other age-related diseases. John's breadth and depth of knowledge in this area will help CRF Health develop industry-leading services for clinical trials these areas.

About CRF Health
CRF Health is a global leader in ePRO (electronic patient reported outcomes) solutions for the life sciences industry. Through innovative technology, a thorough understanding of drug development, and mobile computing, CRF Health is driving the change to higher quality outcomes and more efficient paper-free clinical trials.

CRF Health's ePRO technology has been used in more than 70 countries, on six continents and 68 regional languages, including several regional Indian dialects. CRF Health consistently demonstrates the industry's highest patient compliance rates, while delivering unrivaled data accuracy and unmatched patient and site acceptance.

Since its founding in 2000, CRF Health continues to provide true global ePRO delivery and service. Headquartered in the U.S., CRF Health operates its R&D center of excellence in Helsinki, Finland, and has offices around the world.

For more information, please visit www.crfhealth.com
DaVita Clinical Research® (DCR®), a provider of clinical research services focused on kidney research as well as a multitude of specialty therapeutic populations, has announced the company’s expansion within its Central Laboratory.

DCR’s Central Laboratory is focused on providing world-class clinical research in both complex/specialty populations and therapeutic areas, as well as chronic kidney disease (CKD) populations. By year’s end, the lab’s test menu will increase by 43 percent, maintaining the company’s leadership position in advanced renal care while ensuring critical coverage in the areas of oncology, immunology, endocrinology, cardiology and anemia.

The testing facility has expanded its technology through the addition of two new testing platforms, the IMMULITE 2000 XPi Immunoassay System and the AB SCIEX QTRAP 5500 LC/MS/MS system. Other additions include increased specimen management and storage capabilities for both short- and long-term testing. The Central Laboratory facilitates satisfaction with continuous IT advancements, allowing for clean, timely data and ease of customer access to laboratory results. DCR’s commitment to “Excellence Through Innovation” is evident by its continual, selective additions of scientific and operational staff coming from the CRO and pharma communities.

In addition, DCR recently announced the launch of its Biorepository Services. The biorepository contains collections of biological material and their pertinent databases that are systemized for the purpose of research. This new, one-of-a-kind, state-of-the-art biorepository dramatically improves the odds of a breakthrough discovery by combining samples meticulously collected from our nationwide network of over 1,700 sites richly annotated with patient-level heath information.

“We are proud of our recent investments in equipment and assay development,” stated DCR Vice President of Commercial Development Kevin J. Goudreau. “These investments will allow us to supply central laboratory services outside of renal care. We will continue to invest heavily in assay development until the breadth of our offering covers virtually all therapeutic indications.”
DaVita and DCR are trademarks or registered trademarks of DaVita Inc. All other trademarks are the property of their respective owners.

About DaVita Clinical Research (DCR)
DaVita Clinical Research (DCR) is committed to advancing the knowledge and practice of kidney care. DCR brings unsurpassed knowledge, skill, and expertise to pharmaceutical research, ensuring the success of their clients’ clinical trials. DCR’s clinical expertise ranges from designing the study to preparing and submitting the final report. DCR’s Early Clinical Research unit (Phase I-IIa) and Clinical Development network of physicians and investigative sites, Health Economics and Central Laboratory are focused on providing world-class clinical research in both complex/specialty populations and therapeutic areas as well as CKD and ESRD populations needed to meet clinical goals. To learn more about DCR, visit www.davitaclinicalresearch.com.

About DaVita
DaVita Inc., a Fortune 500® company, is a leading provider of kidney care in the United States, delivering dialysis services to patients with chronic kidney failure and end stage renal disease. DaVita strives to improve patients’ quality of life by innovating clinical care, and by offering integrated treatment plans, personalized care teams and convenient health-management services. As of June 30, 2011, DaVita operated or provided administrative services at 1,669 dialysis facilities, serving approximately 131,000 patients. DaVita supports numerous programs dedicated to creating positive, sustainable change in communities around the world. The company’s leadership development initiatives and social responsibility efforts have been recognized by Fortune, Modern Healthcare, Newsweek and WorldBlu. For more information, please visit www.davita.com.

MedNet Solutions, a global life sciences technology solutions company specializing in clinical study management systems, is pleased to announce the official launch of it iMedNet CRO Partner Program. Designed specifically to help Clinical Research Organizations (CROs) improve research efficiency, expand their service offerings, decrease internal costs and win more business, the program provides CROs with compelling marketplace advantages.

At the core of the program is iMedNet EDC, MedNet's recently released cloud-based, software-as-a-service (SaaS) eClinical solution that allows non-technical clinical research personnel to quickly and easily setup and maintain their own EDC studies. iMedNet EDC's intuitive study configuration tools and form libraries allow studies to be set up in days, not weeks or months. Even entire studies can be replicated in a matter of seconds.

Key additional program features include:

Affordable pricing - iMedNet's CRO Partner pricing model eliminates up front fees and dramatically lowers overall costs making iMedNet EDC practical for all research initiatives - even pre-clinical and phase 1 studies.

Comprehensive iMedNet Designer Training
- MedNet provides a complete iMedNet EDC training and certification program ensuring that all CRO personnel involved in the design and configuration of iMedNet studies are fully versed in the capabilities of the system.

Full Sales and Marketing Support - MedNet directly supports the sales efforts of iMedNet CRO Partners with a complete range of services, from marketing materials and demonstration support, to prospective customer referrals and joint promotional activities.

For more information about MedNet Solutions, iMedNet EDC, or the iMedNet CRO Partner Program, please call MedNet Solutions at (866) 258-2735, email MedNet at This email address is being protected from spambots. You need JavaScript enabled to view it. , or visit www.mednetstudy.com.

About MedNet Solutions

MedNet Solutions is a leading healthcare technology company specializing in electronic data capture (EDC) and clinical study management systems designed for the global life sciences market. Applying critical insight, proven technology and unwavering support, MedNet delivers powerful, flexible and easy‐to‐use web‐based eClinical solutions that effectively support clinical studies, registries and investigator initiated trials. Since 2000, MedNet has successfully supported leading pharmaceutical, medical device, biotechnology, and contract research organizations on clinical research conducted around the world. MedNet delivers a superior customer experience from beginning to end. For more information, please visit www.mednetstudy.com.

Xcelience, a leader in early drug development, has expanded clinical trial supplies manufacturing and packaging capabilities to include four new pieces of equipment and a new fully-automated packaging line.

To complement existing expertise in matrix tablet delivery systems, Xcelience added a MG Futura (capsule-filling machine for powder and pellets), LCI Multi-granulator MG-55 (extruder), QJ-230T marumerizer (spheronizer), and wurster insert (bottom spray) to the  existing Glatt GPCG-3 fluid bed processor. These new pieces enable production, coating and encapsulation of MUDF delivery
systems.

“The new MG Futura is a great example of our continued commitment to add state-of-the-art technology that delivers real value to our clients,” says Theodore Koontz, Director of Operations. “The MG Futura improves upon production times, increases overall capacity, and expands upon our existing capabilities for powders, pellets and powder micro-dosing for inhalation systems”.

In addition, Xcelience has added a fully-automated packaging line (including ink-jet coding) for primary bottling of tablets and capsules. The new packaging line enhances the speed at which batches are packaged, shortens timelines, and enhances our ability to package larger batches of drug product.

About Xcelience LLC

Xcelience is a contract research organization providing formulation development, drug preformulation, analytical, and clinical supplies manufacturing to a global client base since 1997. The company is renowned for reliably expediting early development activities to speed potential drugs to clinical trials while applying stage-specific scientific knowledge and experience. Xcelience's unique corporate
structure creates project teams that work intensively with each client, bringing an extension of their own organization into the Xcelience lab. For more detailed information about Xcelience, visit www.xcelience.com.
Esoterix Clinical Trials Services, a division of Laboratory Corporation of America® Holdings (LabCorp®) (NYSE: LH), today announced a strategic alliance with the David H. Murdock Research Institute (DHMRI) to provide its clients with access to enhanced assay development services. Assays developed at DHMRI for contracted research will be transferred to LabCorp Clinical Trials laboratories worldwide to support global clinical studies. The agreement also provides a mechanism for downstream commercialization of companion diagnostics and other biomarker assays once clinical validation has been established.

“With the addition of DHMRI’s discovery capabilities, LabCorp offers its clinical trials clients the most complete suite of biomarker development tools in the industry,” said Dr. David Johnston, Senior Vice President and Global Head of Clinical Trials at LabCorp. “Our collaboration with DHMRI exemplifies our strong commitment to providing cutting-edge services to our clients,” said Dr. Johnston.

The services available to clients through DHMRI include broad biomarker discovery and proof of concept assay development to support early and late stage drug discovery and development. DHMRI uses trans-disciplinary approaches to provide solutions for customers. DHMRI has capabilities and expertise ranging from profiling at the genetic, biochemical, cellular and in vivo levels to clinical immune system monitoring using multiparameter flow cytometry and multiplexed protein analysis and quantitative gene expression.

About LabCorp®
Laboratory Corporation of America® Holdings, an S&P 500 company, is a pioneer in commercializing new diagnostic technologies and the first in its industry to embrace genomic testing. With annual revenues of $5.0 billion in 2010, over 31,000 employees worldwide, and more than 220,000 clients, LabCorp offers a broad test menu ranging from routine blood analyses to reproductive genetics to DNA sequencing. LabCorp furthers its scientific expertise and innovative clinical testing technology with its Centers of Excellence: The Center for Molecular Biology and Pathology, National Genetics Institute, ViroMed Laboratories, Inc., The Center for Esoteric Testing, Litholink Corporation, Genzyme GeneticsSM*, DIANON Systems, Inc., US LABS, Monogram Biosciences, Inc., and Esoterix and its Colorado Coagulation, Endocrine Sciences, and Cytometry Associates laboratories. LabCorp conducts clinical trials testing through its Esoterix Clinical Trials Services division. LabCorp clients include physicians, government agencies, managed care organizations, hospitals, clinical labs, and pharmaceutical companies. To learn more about our organization, visit our Web site at: www.labcorp.com.

*Genzyme Genetics and its logo are trademarks of Genzyme Corporation and used by Esoterix Genetic Laboratories, LLC, a wholly-owned subsidiary of LabCorp, under license. Esoterix Genetic Laboratories and LabCorp are operated independently from Genzyme Corporation.

This press release contains forward-looking statements. Each of the forward-looking statements is subject to change based on various important factors, including without limitation, competitive actions in themarketplace and adverse actions of governmental and other third-party payors. Actual results could differ materially from those suggested by these forward-looking statements. Further information on potential factors that could affect LabCorp’s financial results is included in the Company’s Form 10-K for the year ended December 31, 2010, and subsequent SEC filings.


About The DHMRI

Established as a nonprofit organization through a private grant by David H. Murdock, the Institute is a catalyst in the development of the North Carolina Research Campus (NCRC) as a world class research facility. Research is performed with nationally-renowned academic and industry partners to understand the mechanistic basis of diseases, to support the development of medicinal or nutritional intervention therapies and to identify potential biomarkers to accelerate the progression of those discoveries into bio-medical practice. The DHMRI’s state-of-the-art technologies include diverse, complementary and integrated platforms in one building to provide unprecedented bioanalytical capabilities including next-generation genetics and genomics advanced characterization of proteins & metabolites using diverse mass spectrometry and immune-approaches as well as having the world’s first actively shielded 950 MHz NMR. In addition, these approaches are complimented by interventional studies in various cellular and in vivo settings. With the acquisition of the Immune Tolerance Institute, the Institute is now supporting numerous clinical trials of immunomodulatory approaches with advanced flow cytometry, immunoassay and gene expression methods across a range of immune related diseases. The broad spectrum of capabilities and expertise resident at the DHMRI and the wider NCRC facilitates an unprecedented level of scientific collaboration and public-private partnership for research at the intersection of human health, nutrition, and agriculture. (www.dhmri.org)
The addition of the Import license saves time, costs and initiates direct communication earlier with clients to expedite early stage clinical studies.

Celerion, the premier provider of innovative early stage drug development solutions, is pleased to announce that its clinical research operations in Belfast, Northern Ireland UK, have received authorization from their competent authority, the Medicines and Healthcare product Regulatory Agency (MHRA) to have importation of IMPs added to their manufacturing (MIA(IMP)) license. The addition to the license enables the elimination of a third party vendor to import IMPs on behalf of Celerion thereby saving time, cost and initiating direct communication with clients to expedite early stage clinical studies.

The import license gives Celerion’s facility in Belfast the ability to import investigational products from outside the European Economic Area when manufacturing standards from the exporting country have been confirmed as equivalent to the standards required by European legislation.

“The addition of the import license was based on client demand and continues to demonstrate the high quality work and experience at Celerion,” said Phil Bach, Vice President of Global Clinical Research at Celerion. “This import license underpins Celerion’s commitment to a global clinical strategy and reduces the lead time from study concept to first dosing. Clients also benefit from reduced costs by eliminating third party storage and transport prior to certification of the product.”

This latest announcement continues to demonstrate Celerion’s commitment to delivering upon the evolving needs of our clients and exemplifies the Belfast team’s commitment to meeting and exceeding our clients’ expectations.

About Celerion
Celerion is the premier provider of innovative early stage clinical research solutions. From facilities strategically located around the world, advanced scientific and technological expertise is applied to clinical research (over 730 beds in Phases 0, I and IIa, NDA-enabling clinical pharmacology, ADME), clinical pharmacology sciences, bioanalytical services (discovery through late stage), and drug development services. Celerion has a full spectrum of resources to meet the needs of the pharmaceutical, biotechnology and generic industries for Phase 0 through IIa proof-of-concept studies. For more information, visit www.celerion.com.
Tuesday, 23 August 2011 04:59

PRA Opens Office In Romania

PRA, a leading Clinical Research Organization, recently opened a new office in Bucharest, Romania to further strengthen our coverage of the Balkan region’s burgeoning markets. The Bucharest office will also support projects in the neighboring Republic of Moldova.

Since 2006, when PRA began conducting clinical trials in Romania, the PRA staff has steadily increased and now includes both product registration and early phase professionals. The number of studies initiated by PRA in this region has more than doubled over the last two years.

“By being based in the Balkan region’s key business and life sciences hub, the Bucharest staff has convenient access to top universities, academic research sites, and most of the country’s major hospitals,” said Ludger Langer, PRA’s Vice President of Clinical Operations in Europe, Asia-Pacific and Africa.

The Bucharest location is the 12th office PRA has opened worldwide since 2009, demonstrating our commitment to meeting our clients’ diverse needs in a dynamic clinical trials environment.

About PRA
PRA is transforming clinical trials through our people, innovation and transparency. PRA provides personalized service customized to the unique requirements of each study. We support our global reach and innovative approach through flexible and reliable service, delivered by skilled employees dedicated to ensuring that sponsors achieve their long-term goals.

We serve our clients across all phases of pharmaceutical and biotech drug development by combining therapeutic and operational expertise with local knowledge. Offering services in 80+ countries and serving sponsors for 30+ years, we have amassed a level of expertise that has enabled us to work on a variety of compounds, ranging from niche treatments and therapies to blockbuster drugs. But at PRA, we are looking to the future, not the past. Our increasingly forward-thinking approach to transforming the clinical trial landscape will continue to make a difference to healthcare patients around the world.

To learn more about PRA, please visit praintl.com, email This email address is being protected from spambots. You need JavaScript enabled to view it. or call our Global Headquarters.
Friday, 19 August 2011 10:09

PRA Strengthens Psychiatry Capabilities

PRA, a leading Clinical Research Organization, announces the hiring of Dr. Frederick T. Lewis, D.O. as Vice President, Psychiatry – Scientific Affairs in our Therapeutic Expertise group. Dr. Lewis will provide medical and scientific support for PRA project teams and guidance to clients in all aspects of clinical drug development.

“Dr. Lewis’s exceptional background in psychiatry and broad-ranging industry experience make him an ideal fit for our Therapeutic Expertise group,” said Dr. Michael Kirchengast, Vice President and head of PRA’s Scientific Affairs department. “Adding Fred to our team of experts strengthens our ability to provide comprehensive strategic consultancy for our clients’ projects.”

Dr. Lewis has more than 20 years of research and professional experience in psychiatry. A graduate of the Pennsylvania State University and the Southeastern College of Osteopathic Medicine, his post-residency experience includes multiple fellowships. Dr. Lewis maintains an appointment as an associate professor at Nova Southeastern University’s College of Osteopathic Medicine, where he chaired the psychiatry department from 1996 to 2003.

Dr. Lewis has received numerous awards, including The President’s Award for Research by Nova Southeastern University. He has served as a consultant and scientific advisor for several pharmaceutical companies and was an original founder of CNS Clinical Research, Inc. Dr. Lewis has been an investigator in numerous clinical trials and authored many publications in the area of psychopharmacology.

PRA’s Scientific Affairs provides access to scientific, therapeutic, drug development and regulatory expertise, which drive the company’s service offerings. Our team of experts facilitates rapid access to investigators, health organizations and patients worldwide. Their relationships with key opinion leaders, regulators, academics and patient advocacy groups form a strong network across the globe.

About PRA
PRA is transforming clinical trials through our people, innovation and transparency. PRA provides personalized service customized to the unique requirements of each study. We support our global reach and innovative approach through flexible and reliable service, delivered by skilled employees dedicated to ensuring that sponsors achieve their long-term goals.

We serve our clients across all phases of pharmaceutical and biotech drug development by combining therapeutic and operational expertise with local knowledge. Offering services in 80+ countries and serving sponsors for 30+ years, we have amassed a level of expertise that has enabled us to work on a variety of compounds, ranging from niche treatments and therapies to blockbuster drugs. But at PRA, we are looking to the future, not the past. Our increasingly forward-thinking approach to transforming the clinical trial landscape will continue to make a difference to healthcare patients around the world.

To learn more about PRA, please visit praintl.com, email This email address is being protected from spambots. You need JavaScript enabled to view it. or call our Global Headquarters.

Bioanalytical Systems, Inc. (Nasdaq: BASI) (BASi) announced today that revenue for the third quarter of fiscal 2011 ended June 30, 2011 increased 5.1% to $8,478,000 from $8,064,000 for the third quarter of fiscal 2010.

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