OmniTrace conducts legal and permissible research of publicly available records and databases where local regulations allow and when appropriate patient consent has been obtained.
For USA searches average turnaround time is 24 – 48 hours. Global searches will vary by country and may range from 7-21 days.
OmniTrace’s clients consist of Pharmaceutical Companies, CROs, AROs, Hospitals, clinical trial sites and government agencies such as the National Institutes of Health.
OmniTrace supported our first study in 2003, and since have successfully handled over twenty-five thousand Lost to Follow-Up related requests globally. OmniTrace is the world’s premier providers of LTFU services.” To “OmniTrace supported our first study in 2003, and since have successfully handled over twenty-five thousand Lost to Follow-Up related requests globally. OmniTrace is the world’s premier provider of LTFU services.
OmniTrace provides comprehensive project support including ICF language review, LTM/CRA/Site LTFU training, IRB and EC response and rebuttals, death certificate retrieval, MAE monitoring, EDC assistance, Site communication, metrics development as well as other custom services.
OmniTrace’s services are available in over fifty countries.
OmniTrace conducts research of publicly available records and databases to identify current contact information or vital status data on subjects who are Lost to Follow-Up or have withdrawn consent. This simple, crucial function significantly reduces missing data that may bias in study results and hinder the regulatory process.
- Significantly reduce the number of LTFU patients
- Determine vital status of those who have withdrawn
- Monitor Major Adverse Events
- Reduce FDA scrutiny
- Maximize clinical trial success
- Eliminate missing trial data
- Allow for a faster clinical trial endpoint
- Enhance regulatory compliance and post study surveillance
- Reduce clinical trial cost