February 24, 2020What's New
We went back to the Target Health website the other day, and under News & Info we clicked on Article, and then on an article from 2012 entitled Lessons Learned From Direct Data Entry. Not only have we continued our commitment to the paperless clinical trial, with no file cabinets or regulatory binders at Target Health, we have regulatory approvals that used our patented solution in the US, Europe and Australia. Now, using Target e*Studio®, you can run your entire clinical trial at one website, starting with Target e*Informed Consent, have the sites perform direct data capture, CRAs completing site monitoring reports, pharmacovigilance performed using our PV module, generation of risk-based monitoring reports, automatic randomization allocation, IMP management, patient and study lock, etc.
The eTMF is managed using Target Document, software we have been using since 2006.
All of our software is 21CFR Part 11 compliant and we have been inspected twice by regulators as part of pre-approval inspections with no Form FDA 483 issued.
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. Also visit the Target Health Eating Website to see all of the fantastic recipes since 2012.
Joyce Hays, Founder and Editor in Chief of On Target
Dr. Jules T. Mitchel, Editor