A full range of services to ensure the integrity of your studies
The growing level of regulatory stringency in drug development demands quality at the highest level. This environment requires the highest attainable levels of quality — no shortcuts, no compromises.
Our global Quality Assurance group recognizes this need and provides a full range of services to ensure the integrity of your studies. We offer:
- Investigative Site Audits
- Trial Master File Audits
- Database Audits
- Clinical Study Report Audits
- Statistical Report Audits
- Vendor Audits
In addition to providing study-specific auditing services to sponsors, our global QA group has a thorough internal audit schedule.