In The News
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1 — 10 of 16 Items
07/09/2009 | Publisher: Pharma Live
Two of Octagon's clinical data strategists co-author chapter in Good Clinical Data Management Practices Guide.
06/23/2009 | Publisher: ClinPage
Octagon Research has been thinking about the entire life cycle of clinical data and regulatory needs long and hard, helping Wyeth and smaller firms.
11/24/2008 | Publisher: Bio-IT World.com
Frank Newby, CDISC's chief operating officer, is gearing up for the training, which he says will differ from the usual training. “It will not be traditional CDISC training on how to create the set up data to be sent to FDA. Instead, it will focus...
11/11/2008 | Publisher: European Pharmaceutical Review
“We are pleased to participate in this year's Asia-Pacific Clinical Trials Congress,” commented Jim Walker, Chairman & CEO, Octagon Research Solutions, Inc. “We decided to lend our support to this year's Congress following our meeting...
11/10/2008 | Publisher: ClinPage.com
Octagon's vision is broader than most technology firms in the industry. It offers a series of systems to handle clinical data and regulatory forms from start to finish or, more specifically, from the moment of data collection, through cleaning and...
11/07/2008 | Publisher: PharmaLive.com
John Lawrie, vice president, Process Solutions at Octagon Research Solutions, Inc. noted, “Evolving global submission standards are adding complexity to the already challenging submission authoring process. Since StartingPoint was first...
11/06/2008 | Publisher: Applied Clinical Trials
Kirk Gallion, president, Octagon Research Solutions, Inc., added, “This is an educated marketplace and one that is seeking real-time solutions from a technology and a resourcing perspective. The ViewPoint Quantum platform...
09/19/2008 | Publisher: PharmaLive.com
“We are pleased to announce the launch of the ViewPoint Quantum website,” noted Kathy Bouldin, senior manager, Marketing, Octagon Research Solutions, Inc. “We believe that the site will help us to develop a strong community using...
09/18/2008 | Publisher: Applied Clinical Trials
“The FDA understands that data standardization is critical to the clinical data lifecycle,” noted Frank Newby, COO, CDISC. “The planned training program demonstrates the agency's commitment to CDISC data standards but also...
09/17/2008 | Publisher: Forbes.com
The Clinical Data Interchange Standards Consortium (CDISC), announced today that the Food and Drug Administration (FDA) selected CDISC, via a formal RFP process, to provide training to FDA reviewers of regulatory submissions.
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