Good Clinical Practice is a set of internationally recognised ethical and scientific quality requirements which must be observed for designing, conducting, recording and reporting clinical trials that involve the participation of human subjects.
Our GCP analytical services support the safety and quality assurance of Investigational Medicinal Products (IMP) and subsequently generated clinical sample analysis in compliance with UK and European legislation (EU Directive 2001/20/EC, article 1, clause 2).
Analytical Techniques Include:
Butterworth Laboratories also offer analytical support for GLP Studies as part of preclinical development for a range of product types.
For more information you can get in touch using our contact form.