Eliminating multiple simultaneous clinical trial enrollments improves research subject safety and data quality. Verified Clinical Trials assigns a proprietary de-identified unique identification code to research subjects, which, combined with other features, tracks clinical trial subjects and the investigational compounds or devices being administered. Incorporating the SAFE-BioPharma standard allows research staff to obtain a digital identity, and the combined service will enable each research subject and trial administrator to apply binding digital signatures to electronic consent forms, patient diaries and other documents.
“Our alignment with SAFE-BioPharma provides Verified Clinical Trials with unique exposure to the SAFE-BioPharma community of companies. Integrating the standard into our service will improve clinical trial efficiencies by eliminating time associated with secure document signing and exchange. It also will reduce trial costs,” said
“The global clinical trial process is undergoing major changes that require more secure and trusted processes. Both Verified Clinical Trials and identity credentials based on the SAFE-BioPharma standard provide intelligent and cost effective alternatives to clinical trial sponsors and CROs,” said
For more information on the SAFE-BioPharma standard for digital identity and digital signatures used in life science and healthcare settings, visit http://www.safe-biopharma.org.
About Verified Clinical Trials
Dedicated to enhancing patient safety and improving data quality by preventing dual enrollment in clinical trials, Verified Clinical Trials provides a unique worldwide clinical trials database registry and a unique yet easy solution to maintain compliance with the complex Medicare Secondary Payer Law. Visit http://www.verifiedclinicaltrials.com
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