Accelerating the Future of
Sites need a remote visit that can differentiate and tell their unique story. A visit by letting CROs/Trial Sponsor explore your site from anywhere on any device.
Is it Pre-Study Visit or Site Initiation Visit
Making Study Start-Up Approval Easier
SiteNavi is a way CROs/Trial Sponsors can tour, select, view and approve a Research site facility and requirements without physically being there. Cost savings for every CRO and Trial Sponsors. Make Site Startup quicker with no travel required. Save time and Save Money.
Facility Approval
Remote tour of the facility to confirm that the site has all the requirements necessary to conduct the trial.
Equipment and Calibration Approval
Identify equipment per room location with a detailed description and an attached calibration record.
Our Capabilities
Delivering unparalleled engagement to provide meaningful data
Fast & Effective
The average PSV/SIV site tour in person visit is 30 minutes to an hour, while SiteNavi remote visit are on average 10 minutes.
Making Visit accessible
Remote clickable photo or videos with elements (such as, equipment's) encourage.
Value & Results
The need for remote visit rises, creating an increase in quality.
Cutting edge made simple
Remote visit engages display calls to action moving start up to the next step in process.
It's time for a better way to approve and engage.
Request Demo
Discover the modern way to approve a Site
Get Started with SiteNavi
Save time and get approved anywhere in the world.
We are SiteNavi
Processes & Solutions
Expedite your site qualification and selection process.
- Through tailored partnership, we help CROs accelerate progress and drive results. Powered by insight and expertise, our solution is designed to solve toughest challenges from cost of travel to meaningful approvals.
- We conduct original best practice research
- Providing continuous study site approval with CRO-focused research to help them reach their goal.
- Getting qualified doctors and sites into research, CROs need to be thinking of overall clinical research portfolio and how they can contribute to the future of research needs.
- Enjoy Business development service for a fraction of what it cost to have CRAs Travel for a tour.
- Maximize your cash flow and profits by removing financial burdens in contract during site study start-ups and uncover all billable items.
- Reduce annual overhead and remove inefficiencies.
- Avoid hefty flight ticket fees.
Improve the site visit experience
The primary objective of a Study startup is to activate the site so that they can ultimately begin collecting data pertaining to the trial.
Waiting Area
Its all starts in the visitors lobby where your are being welcome onsite.
Nurse Station
An area providing request for patients request and care.
Monitoring Room
Dedicated monitoring room for CROs to maintain study confidentiality.
Regulatory & Source Documents Storage
Acceptable Record keeping, retention and document control.
Investigational Product (IP) Storage
Secure location with limited access and temperature controlled room.
Lab Room
Dedicated laboratory room for continuous sample preparation for study clinical trials.
Patient Room
Clinical exam room for centered care.
Doctors Office
Private room for dedicated PIs and or Sub Is on study trials focusing on patient care.
Bringing your CRAs visits together in one platform
Keep track of where, when and who your CRA is conducting a visit with.
- CRA visit tracker
- Visibility to all studies
- Track days on site per monitoring plan
- Eliminate individual CRA calendar
Visit Management Calendar designed for CRO/CRA
- Single feed platform
- Provide collaborative calendar views
- Feature customizable viewing options
(i.e., day, week, month, year)