News Briefs - July 28, 2008


PHT Corp. announced that its LogPad ePRO system is now available on the Windows Mobile platform as well as the Palm operating system. This expands PHT’s portfolio of eDiary devices by adding the Hewlett-Packard iPAQ 210, a slim, wireless handheld device with a high-resolution 4-inch color touch screen. It provides PHT customers and users with a range of benefits, including trustworthy SimpleSend telecommunication options and the ability to support many fonts and languages in global trials. Read the press release.

Medidata Solutions introduced the latest enhancement to its electronic data capture (EDC), management and reporting system, Medidata Rave – the Dynamic Tabulation Engine. This new feature expands Rave’s data-reporting capabilities and further increases the ease and speed at which clinical data can be made available for analysis, reporting and regulatory submissions in sponsor-specific or standards-based formats as they evolve, such as Study Data Tabulation Model (SDTM). Read the press release.

ProTrials Research Inc. has been selected by the Silicon Valley/San Jose Business Journal as one of the area’s Top 50 Women-Owned Businesses for 2008. ProTrials is the only clinical research organization (CROs) to make the Silicon Valley/San Jose Business Journal top 50 and is one of only a handful of women-owned and operated CROs worldwide.  It recently attained certification by the Women’s Business Enterprise National Council, an elite group of women-owned and operated businesses. Read the press release.

At the DIA annual meeting in June, Quanticate introduced itself to the industry as a single entity comprised of two companies: Statwood and Oxford Pharmaceutical Sciences. The integration takes place after five years of collaboration. The company set up its first U.S. operation in Boston in July 2007, and the launch of Quanticate represents the first step in plans to expand the company’s capabilities and presence in the North American market. Read the press release.

 

 

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White Papers & Special Reports

Waters white paper image
Software Helps Doping Control Lab Streamline Results Management
Sponsored by Waters
The Karolinska University Hospital’s Doping Control Lab tests thousands of samples annually for stimulants, diuretics, and other masking agents. Increased regulatory pressure and new technologies increased the number of samples analyzed creating data management challenges. Waters® NuGenesis® Scientific Data Management System and TargetLynx™ Application Manager software were used to reduce the time required to calculate, review and search results.


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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:

  • Assemble data to foster better collaboration
  • Get up-to-date information during clinical trials
  • Make informed decisions earlier in the trial process


BlueArc white paper image
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.

Download this white paper to learn about:

  • Factors driving the data explosion in the life sciences
  • New data management issues that must be addressed
  • HPC trends that are placing new demands on storage
  • Storage solution attributes that address performance, manageability, and energy efficiency.


Life Science Webcasts & Podcasts

Medidata Solutions

Rising Clinical Trial Delays and Costs - Addressing the Cause, Not the Symptoms 

medidata podcastProtocol complexity is taking a toll on clinical study speed and efficiency: increasingly complicated and ambitious protocols are not only burdening sites and study volunteers but are also prolonging trials and increasing expenses. In response, sponsors have turned to global study placement, restructured site relationships and new site management practices, but the problem remains.

This podcast will discuss:

  • Why these responses address only the symptoms, not the underlying cause, of rising clinical trial delays and costs.
  • Results of a recent joint Tufts University / Medidata Solutions study.
  • New metrics benchmarking protocol design trends.
  • Systematic protocol design improvements and why they are essential to clinical trial performance excellence.

Speakers: Ken Getz, Senior Research Fellow at the Tufts Center for the Study of Drug Development, and Ed Seguine, General Manager, Trial Planning Solutions at Medidata.

Download Now 



More Podcasts

Job Openings

Director, Center For Information Technology (CIT) - National Institutes of Health  (NIH), Department of Health and Human Service
Located in Bethesda, MD. This position requires:
• High-level vision, leadership, management, and modernization of CIT programs and services.
• Strategic direction and policy development for CIT long-term operations and objectives.
• Serve as a key IT advisor to the NIH Chief Information Officer.
A TOP SECRET security clearance will be required.  More job detail is found at:  http://www.jobs.nih.gov under the Executive Jobs section.Or contact Ms.Winnie Garner at seniorre@od.nih.gov.  Applications must be received ELECTRONICALLY by (11:59 p.m.), December 17, 2008.  DHHS and NIH are Equal Opportunity Employers

Bioinformatics Manager- Lilly Singapore Centre for Drug Discovery
For more information click here 

For reprints and/or copyright permission, please contact The YGS Group, 1808 Colonial Village Lane, Lancaster, PA;

(717) 399-1900 ext. 125, or via email to Ashley.Zander@theYGSgroup.com.