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BioLegacy Research
About CRO
BioLegacy Research, formerly BTS Research, is a San Diego preclinical CRO.
Frequently Asked Questions
What services does BioLegacy Research offer?
Services include safety assessment, PK/PD studies, custom functional assays, medical device testing and histology. Bioanalytical capabilities include LC-MS/MS, immunoassay platforms, flow cytometry and qPCR. Its disease-model offering includes oncology and inflammatory conditions, allowing efficacy and safety questions to be scoped around the relevant biological system.
What should I include when requesting a proposal from BioLegacy Research?
Describe the therapeutic or device, proposed model, dosing plan and endpoints. State whether the study is exploratory or part of a submission-supporting package.
Where is BioLegacy Research located?
Listed locations include San Diego, CA. Confirm the proposed delivery site when requesting a quote; capabilities may vary by facility.
How can I contact BioLegacy Research through CROaccess?
Use the Contact CRO form or contact CROaccess with your project requirements. CROaccess offers free procurement support to help scope the work, coordinate provider discussions and compare proposals. Research and laboratory services are quoted separately.
Technology & Expertise
BioLegacy Research, formerly BTS Research, is a San Diego preclinical CRO. Its published services combine toxicology, pharmacology, animal-model development and in vitro biology. The company works with both small and large animal species and describes GLP and non-GLP study options.
Core Services
Services include safety assessment, PK/PD studies, custom functional assays, medical device testing and histology. Bioanalytical capabilities include LC-MS/MS, immunoassay platforms, flow cytometry and qPCR. Its disease-model offering includes oncology and inflammatory conditions, allowing efficacy and safety questions to be scoped around the relevant biological system.
Accreditations & Compliance
Confirm the applicable facility, quality system, study standard and required documentation with the provider when scoping regulated work.
