Services
Clinical Quality Assurance & GCP Audits
Quality built into every stage, so your study withstands regulatory scrutiny from inception to database lock.
Request a proposal →Our clinical quality management team works to ICH-GCP and keeps your study inspection-ready throughout. We audit, train and fix problems early, before they turn into findings.
Audits
- Site audits
- Vendor and system audits
- Trial Master File audits
- Audit reports and CAPA follow-up
Systems
- SOP development and review
- Quality management plans
- Inspection readiness and mock inspections
Training
- ICH-GCP training for sites and study teams
- Role-specific training for CRAs, CRCs and auditors
Discuss quality assurance for your study
Tell us about your protocol, timelines and therapeutic area, and we will suggest how ACRS can support it.