A full-service, organized study management. From contract award to study closure
Courier services from LBM to investigator sites, including Chile, Uruguay, Colombia, Perú, Brazil and Mexico
Same-day reporting of pathological results. Short-term or long-term specimen storage
Customized reports and protocol specific databases, remote access and data transfer services
Preparation of customized visit-specific kits, helpdesk, shipping of emergency back-up supplies
The latest technologies applied to testing with the most reliable methods: ELISA, RIA, IRMA, CLIA, HPLC, HPLC MS/MS
LBM is an independent laboratory in Buenos Aires, Argentina, dedicated to clinical biochemistry applied to clinical trials for pharmaceutical companies, CROs, university research departments and other research facilities.
Our capacity and experience enable us to customize our services based on individual client needs and specific study requirements, ensuring high quality results and fast delivery of reports.
We can provide a wide variety of methodologies for the different phases of drug development: enzyme-linked immunosorbent assays (ELISA), radioimmunoassays (RIA), immunoradiometric assays (IRMA), chemiluminescence immunoassays (CLIA), high performance liquid chromatography (HPLC) and high performance liquid chromatography tandem mass spectrometry (HPLC-MS/MS). Through application of these methodologies we also provide analytical services for Bioavailability and Bioequivalence studies.
Our highly qualified staff is proficient in these methodologies applied to clinical chemistry, hematology, immunology, endocrinology, microbiology, virology, toxicology, drug monitoring and DNA analysis.
All procedures and methods are standardized and documented according to GLP (Good Laboratory Practices).
Services offered by LBM for clinical research projects include method development and validation, project management, investigator support, sample management and storage, logistics, properly documented and consistent reference ranges, customized reports, remote data access, data management and FDA 21 CFR, part 11 compliant database.