With services spanning data management, kinetic analysis and report writing, we recognise that our analytical data or report is the final "product" for our clients. They also have to pass the scrutiny of legal forensic investigation and international regulatory authorities and are therefore subject to the same high-integrity quality systems as the data generation itself.

Data management and transfer
HFL's LIMS systems are suited to managing high-throughput routine analyses, single-centre bioanalysis or biomarker projects or complex multicentre, multinational trials involving sample kit management, logistics and sample analyses for clinical safety, PD and PK evaluations. We provide data in any format, including via our secure internet portal Labs@HFL

 

Kinetic analysis
Using the powerful industry standard Kineticaä pharmacokinetic-pharmacodynamic (PK/PD) application for non-compartmental data modelling, HFL can provide a complete bioanalytical PK/TK service to support pre-clinical and clinical studies. HFL have undertaken clinical studies from Phase I to Phase IV across a broad range of therapeutic applications. Our pharmacokineticists are able to provide analyses for bioavailability, bioequivalence studies and the effect of food and gender/age comparisons. Where more detailed statistical analysis and inclusion of pharmacodynamic analysis is called for we have a preferred supplier arrangement with a specialist team of statisticians and kineticists.

Reporting
Whether we are providing non-regulated services, or working to international quality standards such as GLP or GCP, we apply a rigorous approach to quality. We are also flexible in report format, applying either HFL or Sponsor templates according to client and regulator requirements.

Contact us to find out more