In addition to providing in-house Quality Assurance auditing for all clinical trials, the Quality Assurance department provides stand alone services to support companies to develop, implement and maintain quality management systems to assure the highest standard of conformance to GCP, GMP and GLP regulations and to ISO 9000 quality standards.

ICON has the resources to meet all your auditing requirements of Phase I - IV clinical trials. With QA personnel located across Europe and the US, Asia-Pacific, Latin America and Japan, the ICON QA team is flexible enough to provide an individual and personalised service for locally managed projects.

• Phase I - IV GCP audits
• Clinical laboratories (GCP, GLP)
• Database and Statistical tables
• Computer validation
• Clinical trial reports
• Technical and operational vendor audits