Our Services

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 1 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.