Target Health Blog

Why Paperless Clinical Trials, or Should We Say, Why Not?

November 4, 2018

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What's New
Source:

Target e*CTR® (eClinical trial Record), fully integrated with Target e*CRF®, has been used for product approvals in the United States, Europe and Australia. A new program is being launched in Singapore this month. In addition to the international and domestic approvals, one of our clients has requested that Target e*CTR be used in a study so that an adjudication committee can access a limited number “source records“ from the Target e*CTR repository. Of course, access to Target e*CTR is controlled by the study sites.

When direct data entry is linked with risk-based monitoring (RBM), the sites are able to see twice as many study subjects a day, since there is virtually no more work to do once the visit is over. CRAs are also now able to review data, virtually in real time, thus nipping problems in the bud.

The following table says it all:

For more information about Target Health, contact Warren Pearlson (212-681-2100 ext. 165). For additional information about software tools for paperless clinical trials, please also feel free to contact Dr. Jules T. Mitchel. The Target Health software tools are designed to partner with both CROs and Sponsors.

Joyce Hays, Founder and Editor in Chief of On Target

Jules Mitchel, Editor

Contact Target Health

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