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Seven Elements of Clinical Collaboration Integration
Dec 19 | eCliniqua | Guest Commentary | Running a clinical trial in the U.S. is expensive, and document management is one of the most time consuming and costly pieces of the puzzle. The amount of documents, work items, notifications, and other elements of collaboration is growing, resulting in increased management costs and the need to disseminate important information across the organization quickly and efficiently.
Dec 18, 2011
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Raiders of the Lost Protocol—Understanding Past Performance to Predict Future Success
Dec 19 | eCliniqua | Guest Commentary | Protocol complexity continues to increase as studies target ever more narrow patient populations and organizations embrace adaptive designs, in order to do more with less. By thinking of themselves as data archaeologists, today’s protocol authors can leverage the information from previous studies, as well as their operational outcomes, to ensure better protocol design and guarantee operational feasibility.
Dec 18, 2011
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Web Site Visualizes Adverse Events
Dec 5 | News Brief | Nhumi Technologies has unveiled its new web site providing direct access to the safety information of U.S. marketed drugs. The web site presents adverse events reported to the U.S. FDA since 2004. It identifies the most relevant safety information and depicts it on a virtual model of the human anatomy showing body parts that are most adversely affected by a drug.
Dec 5, 2011
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An Inside Perspective on PAREXEL
Nov 22 | Bio-IT World | Mark Goldberg, PAREXEL’s chief operating officer, recently sat down with Bio•IT World chief editor Kevin Davies to discuss the importance of convergence in Perceptive’s suite of eClinical offerings, and to share his insights on the future opportunities, trends, and challenges facing the industry.
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PerkinElmer Targets Holistic Data Solutions
Nov 21 | Bio-IT World | With its recent acquisitions of CambridgeSoft and Geospiza to name but two, PerkinElmer is signaling a new strategy that highlights data analysis and software as much as its traditional strengths in hardware and chemical analysis. Dan Marshak sat down with Bio•IT World chief editor Kevin Davies to discuss PerkinElmer’s evolving strategy from both business and scientific perspectives.
Nov 20, 2011
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New Survey Results Show Asia Pacific CRO Trends
eCliniqua | Guest Commentary | A new survey of contract research trends in Asia Pacific shows mostly small-to-medium contracts in Phase III focused on oncology.
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NuMedii’s New Way to ‘De-Risk’ Drug Repositioning Work
eCliniqua | A newly minted biotechnology company is offering to match the molecular genomic activity of previously approved medicines to that of known diseases to help drug makers find new uses for therapies. “We have two published studies demonstrating [our technology platform] can be used that way, and a third pending publication,” says Gini Deshpande, founder of Menlo Park, CA-based NuMedii.
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Lilly Designs Study to Increase Minority Participation
By eCliniqua Staff September 26, 2011 | Eli Lilly announced the findings from a study designed to increase minority participation in clinical trials last week. The company recognized that racial and ethnic minorities are more likely to develop cancer and
Sep 25, 2011
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Inovio: A Rising Star in the World of Vaccines
September 19, 2011 | In as few as five years, all of the major shortcomings of conventional vaccines will start to vanish as the first DNA-based vaccines hit the market. The vaccines will be remarkably safe and tolerable, easily modified, and cheap to produce in a manufacturing process akin to brewing beer. They’ll also have a long shelf life, maintaining their fidelity even in steamy tropical climates. The development process itself will better integrate scientific inquiry with trial design, so that subsequent vaccines improve with the regularity of an iPhone upgrade.
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Facebook and Pharma – an Uneasy Alliance
September 19, 2011 | On August 15, 2011, Facebook implemented a change in policy that redefines the ground rules for the pharmaceutical industry’s use of this popular social medium. As of that date, pharma companies no longer have the privilege of disabling comment walls on their company-sponsored Facebook pages. The inability of consumers to post or view comments had been a special accommodation from Facebook to the pharmaceutical industry, but no more.
Sep 18, 2011
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Less than 1% of Cancer Patients Enrolled in Trials, Study Says
August 29, 2011 | Less than 1% of cancer patients participate in a clinical trial, according to a study published in the September issue of the Annals of Surgery.
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Trials at the Point-of-Care
eCliniqua | A new type of clinical trial now undergoing testing at the Veterans Affairs (VA) Boston Healthcare System will likely be of interest to emerging accountable care organizations (ACOs) as well as the drug companies that court them. The new approach, most useful in comparative effectiveness research, overcomes the chief disadvantages of the two flanking options: an observational study involving non-experimental treatment decision making or a full-scale, randomized and placebo-controlled trial.
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ClearTrials Releases Study Budgeting Survey Results
By eCliniqua Staff August 4, 2011 | ClearTrial, maker of clinical trial operations software for planning and budgeting trials, released results of a survey earlier this week assessing how life sciences professionals forecast and budget for clinical trials. Almost half of the
Aug 4, 2011
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Cetero Responds to FDA Letter
eCliniqua | On Wednesday, one day after the FDA issued a letter accusing CRO Cetero of "significant violations" at a Cetero facility in Houston, the company responded in a letter on its website.
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Trial Finder Launched for Parkinson's Trials
July 18, 2011 | The Michael J. Fox Foundation for Parkinson's Research has launched a Web-based solution to connect patients with Parkinson's Disease clinical trials. The beta version of the Fox Trial Finder (www.foxtrialfinder.org) compares volunteer information such as location and medical history with trial eligibility requirements to find the best potential matches at study sites nearby. The service matches both people with Parkinson's and control volunteers with the trials that need them.
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DIA 2011—Compliance, Collaboration and the Cloud
By Ann Neuer July 13, 2011 | CHICAGO—This year’s annual DIA meeting featured hundreds of exhibitors and session topics ranging from patient recruitment to cloud computing to improving regulatory reporting. There were several overriding themes including the continuing march towards
Jul 13, 2011
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Using Interim Analyses to Improve Efficiency in Drug Development
Jun 3 | Guest Commentary | Interim analyses offer companies the opportunity to stop studies early when it appears the primary objective will not be achieved or halt trials when there is clear evidence that the primary objective has already been met. This not only lowers costs but also speeds up the time to develop the compound, which obviously benefits both the company and patients.
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Euphoria over EHR/EDC Interoperability May be Misplaced
May 16 | eCliniqua | Despite noble efforts by the Clinical Data Interchange Standards Consortium (CDISC) and others to write a rulebook for the exchange of patient-level clinical information between electronic health records (EHRs) and electronic data capture (EDC), interoperability between the two systems is largely a pipe dream.
May 13, 2011
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MD Anderson Chooses Velos eResearch
May 13 | News Brief | MD Anderson has signed an agreement for an enterprise-wide installation of Velos eResearch for use in clinical trials. The installation is underway now and should be in use by 2012.
May 13, 2011
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eHealth University Unveiled
May 11 | News Brief | This week, National eHealth Collaborative (NeHC) unveiled NeHC University, a revamping and substantial expansion of its NHIN University program.
May 11, 2011