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Clarix IRT Becomes Property of Phase Forward
Bio-IT World | Responding to intense interest among study sponsors and investigative sites for consolidated technologies, Phase Forward invested $40 million in cash to acquire privately held Clarix LLC in early September.
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Pain Relief Studies Drive Growth of Lifetree Clinical Research
Bio-IT World | Lifetree Clinical Research has come a long way since it launched in 2003. Within its first year of business, Lifetree was generating enough profits to build a free-standing clinical research facility.
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BRIDG Moves Toward Double Layer of Semantics
Bio-IT World | Subject matter experts and IT professionals involved in clinical trials should both be happier with the next release of BRIDG, the domain analysis model aimed at synchronizing semantics within the clinical research and healthcare enterprises.
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Briefs – Sept. 29, 2008
- CDISC awarded contract for training of FDA reviewers
- Nextrials expands its executive team
- ACORN appoints Tara Webb senior director of CRO business development
- Good Products and Adlib Software partner in pharmaceutical regulatory submissions
- Paradigm Spine to implement PharmaPros’ automated trial management solution
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Duke Goes with Alphadas for its Early Phase Trials
By Deborah Borfitz Sept. 3, 2008 | Accurate and timely data collection has always been critical to subject safety in first in human clinical trials. It is even more so now that a growing proportion of the Phase I study
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Acurian: Bigger Database, Better Recruitment Results
By Deborah Borfitz Sept. 3, 2008 | In the U.S., the chief challenge of recruiting patients into clinical trials is not disinterest but “putting information in front of people so they can make a choice,” says Rick Malcolm, CEO of
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SAS Takes Lifecycle View of Patient Safety Data
Bio-IT World | The pharmaceutical industry and regulatory agencies are sharpening their focus on patient safety through intense efforts to improve the way safety data are collected, analyzed and interpreted. And there is a long way to go, says Jason Burke, global director of the health and life sciences market segments at SAS.
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Pharsight Broadens Reporting and Analysis Offerings
Bio-IT World | Since its inception 18 months ago, Reporting and Analysis Services (RAS) has turned out to be one of the more active business divisions of the Mountain View, CA based Pharsight Corp.
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Tessella Ready to Release Adaptive Trials Simulator
Bio-IT World | Tessella’s soon-to-launch Adaptive Trials Simulator will be the first opportunity for most sponsor companies to “interact directly” with a Bayesian design of Berry Consultants.
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New Octagon Offerings Provide Just-in-Time Resource Management and Data Validation
Bio-IT World | Octagon Research Solutions aims to bring greater efficiencies to the clinical development supply chain with the launch of its ViewPoint Quantum platform and CheckPoint Data Validation Services.
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|  Managed Innovation, Assured Compliance
sponsored by SAS
Discovery organizations are identifying a lot of promising compounds, but clinical research processes haven't kept pace with timely testing of all those potential therapies. This white paper describes how SAS® Drug Development supports true innovation across the clinical trial process.
In this white paper you will learn how to:
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Addressing Life Sciences Constantly Growing Data Challenges Research Environments
sponsored by BlueArc
The continued explosion of raw experimental data, the increased use of video, the growing adoption of new data retention practices, and the move to high throughput computational workflows are all placing new demands on the way life sciences organizations store and manage their data.
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- Factors driving the data explosion in the life sciences
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- Storage solution attributes that address performance, manageability, and energy efficiency. Download now
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“Storage for Science – Methods for Managing Large and Rapidly Growing Data Stores in Life Science Research Environments” sponsored by Isilon
Large and rapidly growing stores of file-based and other data are a hallmark of life science research and bioinformatics. Determining how best to manage those data stores has become a significant challenge for Researchers and IT Pros alike.
This paper is intended to:
- Provide guidance on the many storage requirements common to Life Science research;
- Explain the evolution of modern storage architectures;
- Summarize the major data storage architectures currently in use.
Additionally, it will present the Isilon IQ clustered storage product as a strong and flexible solution to those needs. Download now
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Adobe
Hospital Paperwork No Longer Has to Be an In-patient Procedure
 How many times have you filled out that same patient registration form when visiting a doctor or the hospital? If you are a hospital administrator, nurse or registrar, you know that your patients and particularly your staff have managed hundreds of consent forms for medication, procedures, anesthesia, and HIPAA. Paperwork redundancy has become a significant bottleneck in the healthcare system. In this podcast, we’ll learn about how Adobe solutions for healthcare can help you streamline your paperwork and stop making paperwork an in-patient procedure.
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Oxford Nanopore Technologies, Oxford, UK
We seek a highly motivated individual to lead the administration, expansion and maintenance of our IT infrastructure, supporting our business operations and technological development of a DNA third generation sequencing system. Includes administration and configuration of core corporate servers, high performance scientific computing and disk systems, security systems, network infrastructure and backups, maintenance of service levels, implementation of any IT related legal compliance issues and policies, and disaster recovery. to apply: www.nanoporetech.com/vacancies
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