Quality Assurance

Trident QA has a highly skilled team whose capabilities extend across several important clinical trial functions.
Our team has specialist experience in both Phase I and later Phase Clinical Research activities.

Contract Audits
Facility audits including document archive and IMP warehouse facilities
Clinical and analytical laboratory audits
Phase I facility and site audits.
Phase II –IV study audits
Device audits
Systems audits and reviews

Training
Audit training
Clinical Trials A-Z (one day course covering monitoring to GCP)

Process Development
Policy and SOP writing and review
Departmental process reviews

Medical Writing Review
Clinical Study Report Reviews
Protocol Review

The Trident Quality Assurance team has a combined 15 years QA experience which includes management, audit and training experience.