Most feasibility tools give you data.
Hyvv gives you a decision.
Provide protocol-like inputs. Get back a ranked, scored, and auditable site list.
Produced by the same scoring engine, every time, whoever runs it.
From
To
- Weeks of cross-referencing
- Multiple platforms
- Subjective calls
- One session
- One engine
- Decision-ready list
why hyvv
You already have access to global datasets and registries.
They give you data to work with. What they don't do is turn it into a structured, weighted, protocol-specific recommendation with a full audit trail.
That's the gap Hyvv was built to close.
01
Protocol-driven site scoring
Every candidate site scored against your specific protocol (indication, phase, patient population, geography), not ranked generically.
02
Competing trial load per site
Live and planned competing trials mapped to each site and PI, so you know what you’re walking into before you commit.
03
PI research & publication fit
PI's scored on phase history and research expertise. Publications are ranked by relevance to your protocol, not just volume or seniority.
04
Country-level epidemiology
Every country scored across patient burden, healthcare infrastructure, and active trial density
05
Deterministic, reproducible output
The same protocol always produces the same site ranking. No variance based on who runs it or which platform they prefer.
06
Full audit trail on every decision
Verified logic for every site rank, providing a defensible and transparent trail for sponsors and stakeholders.
THE OUTPUT
A ranked site list. Full reasoning. Fully documented.
Not a dashboard to interpret. A recommendation you can act on, share with a sponsor, and stand behind.
The recommendation doesn't change based on who runs it
Your junior analyst and your senior director use the same engine and get the same output.
Walk into the sponsor meeting with a score, not an opinion
Every recommendation links back to the drivers that produced it. Fully defensible.
See which sites are already overcommitted
Competing trial load and PI capacity are factored in before you commit, not discovered after.
Show exactly what informed the decision
The data, scoring, and the reasoning are preserved at the point of the decision, retrievable for any sponsor or regulator review.
HOW WE SCORE
What the engine evaluates.
And why it matters.
Hyvv scores every candidate site across four areas of risk, each built from multiple data-driven factors. Not all risk is equal. The weighting reflects that. Weights are configurable per customer protocol.
Site & Capability Match
> Therapeutic area match
> Phase experience match
> Site capabilities match
> Competing trials density
Historical Performance
> Enrolment velocity
> Trial specific performance
> Cross-trial track record
PI Experience
> PI trial history
> Indication specific experience
> Relevant publications
> Study, site & other PI affiliations
Regulatory & Institutional
> Approval timelines
> Execution reliability
> Country regulatory cycle time
> PI trial history
> Indication specific experiences
> Site capabilities match
> Competing trials density
country analysis
Where you run trials matters as much as which sites you pick.
Before Hyvv scores a single site, it models the country landscape across five independent dimensions. The result is a ranked country list detailed breakdown, showing you where to focus before you identify specific sites.
HOW IT WORKS
Protocol inputs in. Ranked site list out. One session.
01
Share your protocol inputs
Indication, phase, geography, patient population, and inclusion/exclusion criteria. Upload a document or walk through it in the platform. Hyvv structures the inputs and queues the analysis.
02
Hyvv runs the engine
The platform simultaneously assesses patient epidemiology, competing trial density, PI experience and research fit, regulatory readiness, and site quality across all relevant countries and sites. Deterministic outputs.
Platform sessions return results within a single session.
Our FaaS offering (where we run the engine on your behalf and deliver a formatted report) takes 7 working days.
03
A deliverable, not a dashboard
A ranked site list, country strategy, PI breakdown, and risk assessment, scored, auditable, and exportable. Ready to take into a sponsor meeting or use for internal sign-off. Every recommendation links back to the data that produced it.
The Intelligence layer
A structured data layer built across sites, investigators and trials.
Hyvv maps relationships across tens of thousands of sites, PIs, indications, and competing studies, and makes them queryable against any protocol in natural language.
Query the data. Don't just receive it.
Data quality & your data
We know public registries have gaps. We cross reference and flag conflicts.
Sources cited on every data point so you can trace where figures come from
Your environment is yours alone. We provide dedicated instances, never visible to others
Sparse data carries a confidence indicator
Transparency is the core of feasibility intelligence.
Who It's For
Built for teams that carry feasibility.
Hyvv maps relationships across tens of thousands of sites, PIs, indications, and competing studies, and makes them queryable against any protocol in natural language.
CROs
"Move faster on every bid. Defend every recommendation."
- Stop cross-referencing multiple sources
- Scored site lists with sourced reasoning
- Give sponsors visibility into selection
- Consistent output across geographies
Biotech & Sponsors
"Come to the table with your own site intelligence."
-
Independent view to evaluate proposals
-
Understand site patient pool and PI capacity
-
FaaS for teams without dedicated feasibility
-
Decisions you can explain internally
feasibility as a service
Not ready for the platform?
Start with a report.
We run the full engine on your protocol and hand you a complete deliverable. No platform licence required.
What you get:
Country Strategy
Ranked country recommendations with regulatory timelines and competitive crowding per market.
Ranked Site List
Every candidate site scored against your protocol, with scores and reasoning shown.
PI Breakdown
Each shortlisted investigator assessed on phase experience and publication relevance to your protocol.
Risk Assessment
Feasibility risks flagged across all dimensions, with mitigation notes for each.
Get a Feasibility Intelligence Report for your next trial.
The fastest way to see what Hyvv produces before committing to a licence. Provide us with a brief and we handle the rest.
Turnaround
7 working days from scoping call.
Output
Site list, country strategy, PI breakdown, risk assessment.
Scope and pricing
Discussed on enquiry based on your protocol.
See it run against a real protocol.
30 minutes. A live scenario. We'll show you what the output looks like for your indication.