Active Clinical Research Execution
Hands-on study execution at our California research site equipped with exam rooms, laboratory facilities, trained clinical staff, and real-time operational oversight.
BioPartners offers full operational execution for clinical studies through our actively enrolling research site in California. As both a CRO and clinical site, we deliver a uniquely unified approach to study implementation—reducing hand-offs, accelerating timelines, and ensuring complete quality oversight.
Our site features:
- Dedicated exam and procedure rooms
- On-site laboratory processing capabilities
- Temperature-controlled sample storage (2–8°C, –20°C, –80°C)
- Secure EDC/EMR systems
- GCP-trained clinical research coordinators and investigators
- Validated SOPs for all study procedures
We specialize in:
- IVD/device performance and usability studies
- Multi-swab comparison studies
- Self-collection and device validation
- Prospective biospecimen collection
- Longitudinal and multi-timepoint sampling
- Rapid enrollment of diverse patient populations
With our integrated CRO + site model, sponsors benefit from real-time communication, immediate issue resolution, strict protocol adherence, and high-quality data generation. Our workflows ensure accurate documentation, consistent biospecimen handling, and full regulatory compliance from the first participant to study closeout.
BioPartners delivers the precision, speed, and reliability required for complex diagnostic and clinical research programs.