With capabilities in the analysis of both chemical and biological entities, HFL has significant experience in evaluating active pharmaceutical ingredients, intermediates and finished products.

HFL provides data for material safety data sheets (MSDS) and batch release documentation for your pre-clinical and clinical development programmes:

•  Impurities
• Degradation products
• Contaminants

Manufacturing Safety & QC Analysis
We also provide manufacturing safety and QC analysis services to determine presence of intermediates, contaminants, impurities or active pharmaceutical ingredients during manufacturing processes as part of your quality control and safety procedures.

Stability Data
We provide chemical stability data on your active pharmaceutical ingredients, intermediates and finished products alone, or in combination with other drugs and/or delivery systems.

Biological and Recombinant Drugs
HFL has dedicated facilities for the analysis of proteins, peptides, antibodies for your biological and recombinant drug products.

Controlled Drug Substances
Licensed by the UK Home Office License, HFL has significant experience in the analysis of a broad range of controlled drug substances in manufacturing processes in a wide variety of matrices.

Quantification and structure elucidation

• HPLC-UV
• GC-MS/MS
• LC-MS/MS
• High-field NMR
• Immunoassay (ELISA, RIA)
• MALDI-MS
• Protein electrophoresis & affinity chromatography