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1608 Centinela Ave Unit 6 Inglewood, CA, 90302 United StatesBioPartners, Inc. is a U.S.-based Contract Research Organization (CRO) specializing in prospective human biospecimen procurement, IRB-governed sample collection, and clinical study support for pharmaceutical, biotech, and diagnostic (IVD) companies. We provide custom, protocol-driven prospective collections across the United States and Eastern Europe through a qualified clinical site network. BioPartners supports diagnostic development, assay validation, clinical performance studies, feasibility programs, and biomarker research. Biospecimen capabilities include: whole blood, plasma, serum, buffy coat, urine, saliva, feces, sputum, NP/OP/nasal swabs, vaginal swabs, gynecological samples, fresh tissue, FFPE blocks, fresh frozen tissue, extracted DNA, and specialty collections from infectious disease, oncology, women’s health, and chronic disease populations. Service capabilities: IRB submission and regulatory coordination ICF and protocol support Site qualification and activation De-identified clinical data collection Cold-chain logistics and global shipping Multi-site enrollment management Quality oversight under ICH-GCP and HIPAA compliance BioPartners operates as a sponsor-focused CRO, delivering flexible enrollment strategies, rapid feasibility, and centralized project oversight. We manage studies from start-up through final shipment, ensuring traceability, compliance, and on-time delivery.
21700 Oxnard #1290 Woodland Hills, CA, 91367 United StatesBioPartners, Inc. is a U.S.-based Contract Research Organization (CRO) specializing in prospective human biospecimen procurement, IRB-governed sample collection, and clinical study support for pharmaceutical, biotech, and diagnostic (IVD) companies. We provide custom, protocol-driven prospective collections across the United States and Eastern Europe through a qualified clinical site network. BioPartners supports diagnostic development, assay validation, clinical performance studies, feasibility programs, and biomarker research. Biospecimen capabilities include: whole blood, plasma, serum, buffy coat, urine, saliva, feces, sputum, NP/OP/nasal swabs, vaginal swabs, gynecological samples, fresh tissue, FFPE blocks, fresh frozen tissue, extracted DNA, and specialty collections from infectious disease, oncology, women’s health, and chronic disease populations. Service capabilities: IRB submission and regulatory coordination ICF and protocol support Site qualification and activation De-identified clinical data collection Cold-chain logistics and global shipping Multi-site enrollment management Quality oversight under ICH-GCP and HIPAA compliance BioPartners operates as a sponsor-focused CRO, delivering flexible enrollment strategies, rapid feasibility, and centralized project oversight. We manage studies from start-up through final shipment, ensuring traceability, compliance, and on-time delivery.
21700 Oxnard #1290 Woodland Hills, California, 91367 United StatesBioPartners, Inc. is a U.S.-based Contract Research Organization (CRO) specializing in prospective human biospecimen procurement, IRB-governed sample collection, and clinical study support for pharmaceutical, biotech, and diagnostic (IVD) companies. We provide custom, protocol-driven prospective collections across the United States and Eastern Europe through a qualified clinical site network. BioPartners supports diagnostic development, assay validation, clinical performance studies, feasibility programs, and biomarker research. Biospecimen capabilities include: whole blood, plasma, serum, buffy coat, urine, saliva, feces, sputum, NP/OP/nasal swabs, vaginal swabs, gynecological samples, fresh tissue, FFPE blocks, fresh frozen tissue, extracted DNA, and specialty collections from infectious disease, oncology, women’s health, and chronic disease populations. Service capabilities: IRB submission and regulatory coordination ICF and protocol support Site qualification and activation De-identified clinical data collection Cold-chain logistics and global shipping Multi-site enrollment management Quality oversight under ICH-GCP and HIPAA compliance BioPartners operates as a sponsor-focused CRO, delivering flexible enrollment strategies, rapid feasibility, and centralized project oversight. We manage studies from start-up through final shipment, ensuring traceability, compliance, and on-time delivery.
6325 Topanga Canyon Blvd Woodland Hills, CA, 91367 2006 United StatesBioPartners, Inc. is a U.S.-based Contract Research Organization (CRO) specializing in prospective human biospecimen procurement, IRB-governed sample collection, and clinical study support for pharmaceutical, biotech, and diagnostic (IVD) companies. We provide custom, protocol-driven prospective collections across the United States and Eastern Europe through a qualified clinical site network. BioPartners supports diagnostic development, assay validation, clinical performance studies, feasibility programs, and biomarker research. Biospecimen capabilities include: whole blood, plasma, serum, buffy coat, urine, saliva, feces, sputum, NP/OP/nasal swabs, vaginal swabs, gynecological samples, fresh tissue, FFPE blocks, fresh frozen tissue, extracted DNA, and specialty collections from infectious disease, oncology, women’s health, and chronic disease populations. Service capabilities: IRB submission and regulatory coordination ICF and protocol support Site qualification and activation De-identified clinical data collection Cold-chain logistics and global shipping Multi-site enrollment management Quality oversight under ICH-GCP and HIPAA compliance BioPartners operates as a sponsor-focused CRO, delivering flexible enrollment strategies, rapid feasibility, and centralized project oversight. We manage studies from start-up through final shipment, ensuring traceability, compliance, and on-time delivery.
21700 Oxnard #450 Woodland Hills, 91367BioPartners, Inc. is a U.S.-based Contract Research Organization (CRO) specializing in prospective human biospecimen procurement, IRB-governed sample collection, and clinical study support for pharmaceutical, biotech, and diagnostic (IVD) companies. We provide custom, protocol-driven prospective collections across the United States and Eastern Europe through a qualified clinical site network. BioPartners supports diagnostic development, assay validation, clinical performance studies, feasibility programs, and biomarker research. Biospecimen capabilities include: whole blood, plasma, serum, buffy coat, urine, saliva, feces, sputum, NP/OP/nasal swabs, vaginal swabs, gynecological samples, fresh tissue, FFPE blocks, fresh frozen tissue, extracted DNA, and specialty collections from infectious disease, oncology, women’s health, and chronic disease populations. Service capabilities: IRB submission and regulatory coordination ICF and protocol support Site qualification and activation De-identified clinical data collection Cold-chain logistics and global shipping Multi-site enrollment management Quality oversight under ICH-GCP and HIPAA compliance BioPartners operates as a sponsor-focused CRO, delivering flexible enrollment strategies, rapid feasibility, and centralized project oversight. We manage studies from start-up through final shipment, ensuring traceability, compliance, and on-time delivery.
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The Contract Research Map is owned and maintained by Scientist.com. It was created to help researchers in the life sciences identify and connect with contract research organizations (CROs) based on geography. Updated nightly, this map features all of the available CROs within our network, so you can order services with a few clicks. Click on a specific country, scroll on the map itself or type into the search bar at the top—there are many ways to find the location and suppliers that you’re looking for. From Argentina to New Zealand, use this map to connect with a CRO near you.
We believe that every researcher across the world should be able to connect with the thousands of global CROs that exist and have the opportunity to work together. Like many industries,the life science supply chain has been disrupted over the last year. But there are many other circumstances such as international customs regulations or sensitive shipping times that create limitations around which countries are feasible to partner with. Sometimes, finding a CRO based in a country that best suits your research needs is imperative. We hope this contract research map allows you to find the right partner in the right place at the right time.
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