GCP Analytical Services

Good Clinical Practice (GCP) compliant analytical services for the testing and evaluation of clinical trial samples employing a wide range of analytical technologies from mass spectrometry, chromatography and more.

The Medicines for Human Use (Clinical Trials) Regulations 2004 (the Regulations) regulate the conduct of clinical trials in the United Kingdom. The regulations relate to persons or organisations that participate in any aspect of a human clinical trial including organisations that analyse or evaluate samples collected as part of a clinical trial. It is essential that sample analysis or evaluation is performed to an acceptable standard which will ensure patient safety is not compromised and that data is reliable and accurately reported.

Intertek operates to GCP, GLP and GMP quality standards and maintains its own quality systems via a dedicated and independent Quality Assurance Unit. GCP compliant analytical services are available across a wide range of analytical technologies and delivered via experienced Regulatory Project Managers in a professional and efficient manner.

Intertek also holds a Human Tissue Licence, regulated and inspected by the Human Tissue Authority (HTA), facilitating analytical studies to support our client’s clinical research programmes.

Request more information to see how Intertek can help your organization with GCP Analytical Services.