Founded over thirty-eight years ago, DRS Corporation remains one of the leaders in the clinical study and samples management verticals.
DRS is proud of our reputation for delivering solutions to global life science organizations of all sizes and supporting clinical drug trials around the world. Our patented sample management product has been assisting organizations since 1990 with maintaining PDMA compliance for drug sample distribution. Our developed products align the latest software technology with an exceptional operational management service.
Our proprietary eTMF platform provides a simple workflow for users across the globe and our professional services support team assists clients with the daily processing and quality control (QC) of their data.
DRS’ partners have also relied on us to transfer study data from the originating system to any format that is specific to their internal platform.
Reach out to us today to discuss how DRS can service your organization's needs! info@drscorp.com
Industry
IT Services and IT Consulting
HQ Location
1435 Morris Ave
Suite 2G
Union, NJ 07083, US
Keywords
Electronic Trial Master File (eTMF) SoftwareStudy Archiving PlatformClinical Study Transfer and Migration ServicesDocument Quality Control (QC) Processing and AttributioStudy Oversight and Inspection SupportStudy Content ReviewsPaper Scanning Services and CertificatioTMF Reference Model IndexingPDMA Sample Management Software SolutionsSample Reconciliation and Audit Services