Services
May the scientists need human biospecimens for their study, we offer the most effective & convenient solutions
BioPartners Inc. provides comprehensive, end-to-end clinical research solutions designed to accelerate timelines, ensure data integrity, and support the successful development of pharmaceuticals, diagnostics, and medical devices.
Our unique structure — combining a full-service CRO with an actively enrolling clinical research site — allows sponsors to streamline operations, reduce hand-offs, and gain full visibility across every phase of execution.
Whether you require feasibility, clinical operations, biospecimen support, or complete study management, BioPartners delivers the scientific rigor, operational precision, and regulatory alignment needed for exceptional outcomes.
Full-Service Clinical
Research (CRO)
BioPartners provides end-to-end clinical trial management for Phase II–IV studies, IVD/device performance evaluations, and observational research. Our team oversees every step—from protocol design and feasibility to regulatory submissions, monitoring, data management, and study closeout.
Sponsors benefit from seamless communication, real-time visibility, and high-quality, audit-ready deliverables.
Active Clinical Research
Execution
BioPartners conducts hands-on study execution at our independent clinical research site in California, equipped with dedicated exam rooms, laboratory processing space, temperature-controlled storage, and GCP-trained clinical staff.
We specialize in precise sample-driven workflows, IVD/device performance studies, multi-swab comparisons, self-collection device evaluations, and longitudinal sampling.
Our integrated model ensures fast study activation, consistent protocol adherence, and real-time oversight for reliable, audit-ready results.
Biobank &
Human Biospecimens
BioPartners provides high-quality, ethically collected biospecimens to support diagnostics development, biomarker discovery, and clinical research. We offer prospective and retrospective collection, complex processing (plasma, serum, PBMCs, swabs, urine, saliva), temperature-controlled storage, and global IATA-compliant shipping.
Every sample includes detailed clinical metadata, chain-of-custody documentation, and validated processing workflows to ensure integrity and reproducibility.
Supporting
services
BioPartners provides a comprehensive suite of supporting services designed to enhance study performance, accelerate timelines, and ensure regulatory compliance across clinical and diagnostic research programs.
Diagnostic & IVD Performance Studies
Expert support for sensitivity/specificity evaluations, comparator method testing, CLIA-waived pathways, usability studies, and enrollment of both symptomatic and asymptomatic populations.
Clinical Operations & Site Management
Study start-up, patient flow coordination, monitoring support, delegation oversight, and complete TMF and documentation management.
Regulatory Affairs
Full IRB/EC submissions, ICF development, safety reporting, regulatory updates, and alignment with FDA, ICH-GCP, HIPAA, and GDPR standards.
Patient Recruitment & Retention
Access to diverse populations, rare disease cohorts, healthy volunteers, and targeted recruitment strategies to maximize enrollment and retention.
Biospecimen Processing & Logistics
Validated processing workflows, aliquoting, stabilization, controlled-temperature storage, full chain-of-custody, and global IATA-certified shipping.
