On-site analytical services, provided by our dedicated laboratory team, offers support to the entire clinical development programme both large and small molecule, through to Phase III and post-marketing studies.
Our experienced project scientists can help you get the most from your study. Expertise in biomarkers and the flexibility to adapt and develop validated methods tailor-made to client’s requirements ensure that you get the results you need, when you need them.
For further information please contact enquiries@lcg-bourn.co.uk.
Specialist laboratory services
Particular strength in endocrinology and cytokine analysis
- Comprehensive immunoassay capability
- Extensive database of reference data
- Method validation to FDA specification
Biomarker services
Flow cytometry for multi-analyze assays and cell surface markers
- Intra-cellular signalling
- Functional assays
- Proteomics
Routine laboratory services
Routine laboratory services
- Rapid turnaround
- Comprehensive test repertoire
- Flexible data format delivery
Quality
Quality underpins all that we do. Operating to the quality standards of ICH GCP, and to the principles of GLP, every project is subject to rigorous internal quality control systems and procedures. Our laboratories have been successfully audited by the MHRA and FDA, as well as numerous sponsors. We also participate in the UK external quality control scheme, NEQAS.
Service
The laboratory provides analytical data ranging from routine safety parameters through to specialist pharmacokinetic and pharmacodynamic markers. To complement analytical support, we offer our clients a number of additional services including method development, validation and protocol preparation, data management and reporting.
Management
We appoint a dedicated team for every project to include an experienced project scientist and a study coordinator. This approach ensures clear lines of communication with our clients and manages scientific and logistical aspects of each project to meet agreed deliverables.