Gcp Bioanalytical services

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Intertek offers wide range of pharmaceutical services which includes GCP Bioanalysis to support your clinical research.
Good Clinical Practice (GCP) is a set of internationally recognized, ethical and scientific quality requirements which must be observed for designing, conducting, recording and reporting clinical trials that involve the participation of human subjects (EU Directive 2001/20/EC, article 1, clause 2).  GCP bioanalytical services support clinical trials that are required to comply with UK and European Legislation. 

Our bioanalysis laboratories offer both GCP and Good Laboratory Practice (GLP) bioanalysis contract services to support preclinical and clinical development for a range of product types including small molecule pharmaceuticals, proteins and PEGylated products. GCP bioanalysis services are available across a wide range of bioanalytical technologies, and delivered via our team of experienced Regulatory Project Managers.  It includes bioanalytical technologies, bioanalytical method development and validation, clinical sample analysis (human plasma and urine), pharmacokinetic (pk) and pharmacodynamic (pd) bioanalysis for small molecules and biologics, metals and inorganic bioanalysis, etc.

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