LC-MS method development and validation expertise for Good Laboratory Practice (GLP) bioanalysis studies since 1990
Bioanalytical LC-MS method development for quantitative determination of drugs and their metabolites in biological fluids is crucial during drug development. LC-MS uses its sensitivity and specificity to detect and quantify compounds accurately. The need for efficiently generated, regulatory compliant bioanalytical data is reliant on fit-for-purpose methods being developed and validated by experienced LC-MS scientists.
LC-MS uses
Our bioanalysis LC-MS method development teams are recognized for the ability to efficiently develop and validate routine and non-routine methods in a wide variety of matrices and uses, and to rapidly employ these assays in a GLP-compliant, high throughput sample analysis environment.
As pioneers in applying this technology to quantitative analysis for Good Laboratory Practice (GLP) studies, our extensive lab background and expertise combined with a high level of commitment to customer service, have established Intertek as a premier bioanalytical LC-MS resource for the pharmaceutical industry.
LC-MS method development lab expertise includes:
- Liquid/Liquid, SPE and Protein Precipitation in 96-Well and Standard Formats
- Hydrophilic Interaction Chromatography (HILIC)
- Ion Exchange Solid Phase Extraction (SPE) and Chromatography
- Chiral Analysis
- Analysis of Drugs in Ocular Tissues
- Biodistribution studies
- Analysis of Peptides and Pegylated Drugs and Metabolites
- High Throughput Automated Liquid handling Using Hamilton Microlab StarLET Systems
Partner with our expert LC-MS method development team for reliable, GLP-compliant bioanalysis—contact us today.
Related Method Development Services

Pharmaceutical News & Events
- PRESS RELEASE! Intertek partners with CrystecPharma to advance formulation science and accelerate development for dry powder inhalers
- NEW! Blog: Optimising Quality in Pharma Supply Chains
- Determination of Particles in Pharmaceuticals - Article
- Discover our Audit Live Tool for direct access to our scheduled audits
- Extractables/Leachables Lab Tour - Request access
- Medical Device Extractables & Leachables Studies
- Glycosylation Analytical Approaches for Antibody Therapeutics
- Rapid Determination of Low/Trace Level Benzene in Pharmaceutical Excipients and Finished Products
Bioanalysis and Biopharmaceuticals Webinar Series
Register now for these webinars
- Drug tolerance in immunogenicity testing
- Comparability studies for biosimilar antibodies
- Bioanalysis and immunogenicity assays for biosimilars
- Regulatory considerations for nonclinical development of antibodies
- Potency testing for a biosimilar antibody
