Give sites hours back.
Give your study weeks back.
OptiSite replaces email-and-Word document feasibility with one connected workflow. Sites reuse what you already know, confirm what changed and focus on the questions that actually depend on the study. Study teams compare sites side by side, surface risks earlier and make selection decisions they can stand behind.
Built on 14 years of clinical technology delivery across 100+ global studies.
Feasibility still runs on email. Everyone pays for it.
Sites keep answering variations of the same questions. Study teams keep chasing spreadsheets, comparing inconsistent responses and piecing together why one site was selected over another. The cost shows up in time, quality and decisions.
Built for the people who carry study start-up.
One workflow, three sides, no more chasing attachments.
Launch feasibility in minutes
Build questionnaires from your controlled library, publish to every site at once, and watch responses arrive structured and comparable in real time.
Select sites you can stand behind
Suitability signals, risk flags and side-by-side comparison turn selection meetings into decisions, with reasoning captured as you go.
Answer once. Be ready for the next study.
A living site profile pre-fills what sponsors keep asking. Site teams confirm what changed and spend their time on the questions that really matter for this study.
From protocol synopsis to site decision, in one place.
Build questionnaires in minutes, not meetings.
Standard questions come out of the box. Your own library stays private, reusable and version-controlled, so every study starts from what already works.
Sites answer once, then confirm what changed.
Living site profiles cover facilities, technology, staffing and regulatory readiness. Smart reuse pre-fills known answers with freshness checks, and role routing sends each question to the right person.
Decide with evidence, not email archaeology.
Structured responses arrive comparable across sites and countries. Suitability confidence and risk flags focus attention, and every clarification stays attached to the answer it belongs to.
Four steps. Weeks recovered.
The questions do not need to change overnight. The way you run feasibility does.
Attach the synopsis
Sites review the protocol synopsis before they answer, so responses reflect the study you’re actually running.
Publish from your library
Assemble, version and approve the questionnaire, then publish to every site in one action.
Sites confirm and respond
Known facts arrive pre-filled. Sites confirm what changed and focus on the study-specific questions.
Review, decide, document
Compare responses side by side, resolve queries in context and save decisions with a full audit trail.
Inspection-ready by default.
Site selection should not become a black box once the emails, spreadsheets and meeting notes disappear. OptiSite keeps the questionnaire, responses, clarifications and selection reasoning connected from start to finish.
Immutable versions
Published questionnaires are locked. Every assignment binds to the exact version a site received.
Append-only audit trail
Every workflow event recorded and attributable, from publication to final decision.
Controlled changes
Post-submission edits require a change comment and route back through study team review.
Role-based access
Sites see only their sites and studies. Reviewer guidance never leaks to site users.
Export for filing
Site responses export to PDF for your TMF, with decisions and reasoning attached.
Your library stays yours
Platform questions are shared. Your sponsor library and your sites’ responses are private to you.
Data residency to your requirements
Validation documentation available on request
“Feasibility is the first conversation a sponsor has with a site. OptiSite makes it a conversation worth having, for both sides.“
OptiSite brings together 14+ years of experience delivering clinical technology across sponsors, technology providers and more than 100 global studies. It is built around the same principles that have shaped OptiTrial from day one: make technology easier for people to use, give teams better information and design the process around how trials actually work.
- 14+ yearsClinical technology leadership
- 100+ studiesGlobal clinical technology delivery
- AstraZenecaFormer Head, Digital Patient Solutions & Emerging Technology
- PharmaTimesInternational Clinical Researcher of the Year – DCT
What study teams ask us first.
What exactly is OptiSite?
How does it reduce burden on sites?
Is our question library shared with other sponsors?
How does OptiSite support inspection readiness?
Where is our data hosted and how is it protected?
How do we get started?
Site selection should not run on email.
See what feasibility looks like when sites do not start from scratch, study teams can see the evidence in one place and decisions do not disappear into inboxes.
We are onboarding a small group of founding sponsors and CROs now. Early partners get direct input into the platform, analytics and roadmap.