DaVinci Research
Clinical research site and Site Management Organization (SMO) based in Roseville, CA that conducts investigator‑initiated and sponsor/CRO‑sponsored clinical trials across pharmaceutical and medical device programs. Services include site management, patient recruitment and enrollment, regulatory documentation, and clinical project management. The organization operates a patient‑facing clinic environment and partners with investigators and sponsors to execute multicenter trials.
Industries
Nr. of Employees
small (1-50)
DaVinci Research
Products
Clinical Trial Participation Services
Provides patients the opportunity to enroll in clinical trials to access investigational treatments and contribute to medical research.
Clinical Trial Participation Services
Provides patients the opportunity to enroll in clinical trials to access investigational treatments and contribute to medical research.
Services
On‑site clinical trial conduct including participant visits, consenting, clinical assessments, and in‑office procedures for sponsor and CRO studies.
SMO services to manage study start‑up, sponsor communications, logistics, and site operations across trials.
Assignment of project management resources to plan, schedule, and oversee study activities and milestones.
Source data capture, regulatory file maintenance, and preparation of documentation to meet sponsor and regulatory expectations.
On‑site clinical trial conduct including participant visits, consenting, clinical assessments, and in‑office procedures for sponsor and CRO studies.
SMO services to manage study start‑up, sponsor communications, logistics, and site operations across trials.
Assignment of project management resources to plan, schedule, and oversee study activities and milestones.
Source data capture, regulatory file maintenance, and preparation of documentation to meet sponsor and regulatory expectations.
Expertise Areas
- Clinical trial management
- Site management organization (SMO) services
- Patient recruitment and retention
- Regulatory compliance and FDA/IRB preparedness
Key Technologies
- Multicenter randomized controlled trial conduct
- Investigator site operations for device and pharmaceutical studies
- Clinical participant recruitment and screening methodologies
- Regulatory documentation and audit preparation processes
News & Updates
Press article featuring the organization.
Press article featuring the organization.
Press article featuring the organization.
Press article featuring the organization.