ICON has the resources to meet your requirements of Phase I - IV clinical trials

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.

Our QA services encompass the following:

  • Auditing
  • Phase I facilities
  • Phase I - IV GCP audits
  • Clinical laboratories (GCP, GLP)
  • Database and Statistical tables
  • Computer validation
  • Clinical trial reports
  • Pre-FDA/regulatory inspections
  • Quality Systems Development (GCP, GLP)

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.