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Grunenthal Expands Use of BioClinica's Next Generation Trident IWR/IVR for Global Trial
Date:6/20/2013

ion of Trident expands Grunenthal's use of BioClinica solutions, specifically OnPoint CTMS. In March 2012, the pharmaceutical company penned an agreement to use the customizable clinical trial management system enterprise-wide for gathering and sharing clinical trials information. Grunenthal made the selection recognizing OnPoint CTMS could help further innovation and development of new pain therapies.

"We are very pleased Grunenthal is expanding its use of BioClinica products to include Trident," said Peter Benton, BioClinica's President of eClinical Solutions. "The BioClinica suite of eClinical solutions is designed especially for this kind of integration, and will help Grunenthal manage its future clinical trials more efficiently."    

Trident reduces the average time it takes to write, set up, and validate IWR and IVR protocols from months to weeks. Trident supports all of a sponsor's clinical studies within a standardized data model that better supports automatic drug pooling and reporting.  By giving clinical trial sponsors the ability to monitor and maintain all their study protocols in one place, it is more efficient and cost-effective than developing specifications, programming and validating a new IWR system for each new study.

BioClinica is offering a free webinar on the subject of controlled substance studies titled Controlled Substance Studies: Meeting the Supply Management Challenge on August 8th, 2013 at 11:00 AM Eastern Time. BioClinica representatives will also be available to demonstrate the company's leading eClinical solutions at the Drug Information Association annual meet
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SOURCE BioClinica, Inc.
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