A streamlined study process so you can focus on results
Advantages our trial process offers Sponsors
Expedited study start up
Our streamlined study start up process means that sites can start enrolling patients earlier.
Complete IRB submission
Our regulatory specialists handle all aspects of Institutional Review Board requirements.
Dedicated site training
Our accessible research teams train sites to reduce potential non-conformance issues.
Broad patient representation
Our nationwide network enrolls patients across different ethnicities and socioeconomic classes, ensuring a rich diversity of patients.
Timely data entry
Yanuvia’s electronic document platform ensures that patient data promptly reaches Yanuvia.
Quality assurance
We are ISO-9001 certified, so we know how to conduct internal and external audits, helping maintain data accuracy.
Full protocol compliance
As part of Yanuvia’s QMS, we have established CAPA processes in place.
Trial master file
Yanuvia’s proprietary EDC (YDECSTM)serves as a trial master file, allowing for remote monitoring.
CITI program credentialed
All Yanuvia team members have completed industry-standard Collaborative Institutional Training Initiative courses.
Dedicated support staff
Our clinical research professionals are at your service whenever live assistance is needed.
"I was drawn to clinical research by its important contributions to healthcare — yet it was clear there was a need to make the process less stressful and more efficient. The Yanuvia team is proud to be doing just that, day after day after day."
Hillel D. Cohen, M.D.
Chief Executive Officer and Founder
Our ISO certification is your quality hallmark
