Phase Clinical is an innovative biospecimen and clinical trial service provider, specializing in a broad global network of oncology sites and in-house scientific expertise to tackle custom prospective projects at competitive prices.

Study Protocol Development
We work with you to plan and document how the trial should be conducted, including objectives, methodology, analysis, patient enrollment, and provisions for data quality and integrity.
Our patient availability data gives sponsors information up front for planning and conduct.
Phase Clinical Services provides expertise in adaptive clinical trial protocol development.
Site Recruitment
Sponsors gain exclusive access to our network of sites strategically selected for:
Strong oncology focus at hospital oncology centers or departments
Doctors and staff qualified and eager to participate in Phase 0-II oncology research
Available oncology patient pools and organized patient data
Full compliance with FDA and EMA standards
Access to advanced equipment and technology
Untapped capacity for research participation due to unsaturated markets for clinical trials
IRB Approval & Amendments
Phase Clinical Services can expedite approval as quickly as one month when working through our network.
We facilitate and expedite the IRB amendment process.
Patient Recruitment
Sponsors gain access to over 50,000 oncology patients per year, already identified as available in our network.
Staff Training
We minimize sponsor needs for training and oversight. Our local teams interact directly with staff to ensure protocols are implemented correctly.
Data Management and Biostatistics
Sponsors can realize significant cost efficiencies with clinical data management services, which provide high data quality, data integration and availability.
Our full-service model provides the flexibility, agility, and speed you need for cancer drug and device development, so you can deliver more effective therapies to doctors and patients.