Fast-Track Trial Start-Up. Protect Site Bandwidth. Keep Participants First.
Navora reduces start-up friction by aligning sponsor expectations with site realities—delivering lean, hands-on support that keeps your team focused on care
Navora reduces start-up friction by aligning sponsor expectations with site realities—delivering lean, hands-on support that keeps your team focused on care
Support Where It's Needed Most
Sites
Sponsors
CROs
IRB submissions, amendments, contracts, budgets, and documentation handled with care
Workflows designed to protect bandwidth and reduce burnout
Accelerated start-up reduces delays for faster activation
Real-time clarity with shared trackers and dashboards
Seamless integration into oversight and reporting
A partner who enhances—not duplicates—your operations
Where Start-Up Stalls
Documentation shifting without clear communication
Teams duplicating effort instead of moving toward activation
Mid-course amendments adding unexpected complexity
Lack of clarity on who owns activation tasks across functions
IRB submissions delayed due to missing or unclear materials
Sponsors, CROs, and sites speaking different “system languages”
Unclear expectations or handoffs between stakeholders
Our Approach
We prep study documents and submissions early, keeping start-up on track once agreements are final.
Simple tools slot into your current workflows—no new portals, no reinvention.
We listen first. Every process reduces site burden, keeps sponsors informed, and accelerates first-patient-first-visit.
We prepare complete, inspection-ready IRB packets and perform thorough quality checks to prevent delays from missing or inconsistent documents.
We coordinate amendment submissions, map their impact across documents, and keep stakeholders aligned to minimize disruption and rework.
We implement streamlined filing and version control, ensuring every stakeholder works from the same up-to-date source with zero duplication.
We facilitate clear, consistent messaging between sponsors and sites, reducing misaligned expectations and unnecessary queries.
Streamlined contracts and budgets—protecting your resources, avoiding delays.
Shared Activity Trackers & Dashboards
We provide real-time, transparent tools that track submissions, approvals, and progress—keeping all parties on the same page.
We manage site start-up milestones step by step, so activation is achieved quickly without overloading site staff.
We co-design efficient workflows and tools tailored to lean site site teams, avoiding unnecessary systems and keeping the focus on participants.
When activation is smooth, participants gain faster access to trials—and that’s the outcome that matters most.
Faster site activation → accelerated start-up, bringing therapies to participants quicker and reducing cost of delays
Transparent → real-time alignment across stakeholders
Less duplication → lighter workload and fewer queries
Protected site bandwidth → focus on participants, increase enrollment and data integrity
Strategic partnership → for sites, sponsors, CROs, and emerging biotechs
From Intake to Activate in 4 Steps
Navora Reviews and Reaches Out
We assess your intake and follow up with tailored next steps.
Co-Design Your Workflow
Together, we adapt tools that fit your systems
Execute and Iterate
We guide your team through study start-up. Post-launch, we’re available for amendment support or re-engagement
We'll reach out within 1 business day