EFIC CONSULTING AND OPERATIONAL SUPPORT
EFIC expertise. Practical support. Stronger trial implementation.
EFIC Support helps investigators, sponsors, and coordinating centers plan and implement clinical trials conducted under exception from informed consent.
Experience built for complex emergency research
EFIC studies require rigorous science, sound regulatory strategy, meaningful community engagement, and disciplined execution across every participating site. EFIC Support brings those elements together in one coordinated approach.
25+ years
Experience in emergency care, prehospital research, clinical trial coordination, and EFIC implementation.
250+ centers
Centralized CC/PD support delivered across more than 250 participating academic centers.
9 protocols and networks
Operational experience spanning distinct multicenter emergency and trauma research programs.
Core services
EFIC strategy and planning
Early consultation to align protocol requirements, regulatory expectations, timelines, and operational feasibility.
Community consultation and public disclosure
Centralized campaign development, community engagement, survey implementation, documentation, and reporting.
Multicenter implementation
Scalable support for coordinating centers and participating sites, from activation through final public disclosure.
Support designed for your role
Investigators and research teams
Translate an innovative protocol into a defensible and workable EFIC plan. Anticipate regulatory questions, reduce avoidable delays, and prepare sites for consistent implementation.
Sponsors and coordinating centers
Build a standardized national approach while respecting local communities and IRB requirements. Centralize materials, reporting, and operational support across the network.
Start with the right EFIC strategy
Early planning can clarify requirements, identify operational risks, and establish a practical path from protocol development to site activation.
