Study Start‑Up
Rapid feasibility, site selection packages, IRB coordination, and contract/budget execution.
- Feasibility & pre‑screening
- Regulatory submissions
- Contracts & budgets
Full‑stack site support for Phase II–IV, devices, vaccines, and observational studies.
Partner With UsRapid feasibility, site selection packages, IRB coordination, and contract/budget execution.
Community outreach, bilingual call center, and EMR‑assisted pre‑screens for qualified referrals.
GCP‑compliant visits with vitals, EKGs, labs, IP accountability, and deviation tracking.
eSource/ePRO ready, remote monitoring support, and 100% source‑to‑CRF verification.
AE/SAE reporting, DSMB coordination, and secure PHI workflows aligned to HIPAA.
Robust SOPs, staff training, and version control for protocols, ICFs, and logs.
We collaborate with board‑certified investigators across multiple indications.
Feasibility, CTA/budget, and IRB submissions to launch on time.
Targeted outreach and prescreening to meet enrollment goals.
Protocol‑driven procedures, IP control, and real‑time data entry.
Query resolution, reconciliation, and inspection‑ready files.
Send us your protocol synopsis or feasibility questionnaire. We’ll turn around quickly.
Contact Our Team