Illustrated clinic wing with offices, a laboratory and a sample cooler in transit

Contract Research Organizations

Make your scientific expertise the reason sponsors choose you

Altrovia turns your expertise, evidence and sponsor requirements into agentic workflows for stronger proposals and smoother sign-off.

Scale your expertise across every sponsor engagement

Proposals

Show the thinking that sets your bid apart

Bring sponsors a working design with endpoint options, eligibility considerations, supporting evidence and explicit trade-offs. Make your recommendations tangible before the engagement begins, so sponsors see the quality of your thinking, not just your credentials.

Delivery

Give your experts more capacity to deliver

Let agents gather evidence, run cross-checks and coordinate review, while your writers and specialists focus on scientific judgment. Keep sources and decisions beside the protocol, so expert teams have more capacity and every call stays with a person.

Sponsor alignment

Give sponsors a clear path to sign-off

Bring sponsor requirements, questions, changes and approvals into one shared workflow, with comments tied to clauses and changes routed for approval. Both teams stay aligned on what changed, why, and what still needs a decision.

Projected delivery targets

More value from the expertise you already have

Projected targets for a CRO design service delivering approximately forty protocols annually, assessed against its delivery scope and baseline.

25%33%

Target gross margin for the same scope

50%

Target reduction in sponsor queries per protocol, compared with the team’s baseline

+15%

Target improvement in bid win rate

6 weeks

Target median delivery time to sponsor sign-off

Projections, not measured results. Actual outcomes depend on the engagement mix, the team’s baseline and execution.

Turn your delivery methods into reusable workflows

Connect your internal methods, reusable guidance and sponsor materials. Altrovia gives agents the right context for each engagement, alongside public evidence and within each sponsor’s permissions.

Your organization / Data sourcesPrivate to your team
  • Your methodsConnected
  • Reusable guidanceConnected
  • Sponsor permissionsConnected

From conversations with CRO teams

“We review 100–200 trials to find the 20 that will actually inform the protocol.”
CRO, Medical Writer
“We draft in Word, circulate it for internal review, then send it to the sponsor for another round of comments.”
CRO, Medical Writer
“Scientific, commercial, and regulatory teams come into the design process with different expectations that need to be reconciled.”
CRO, Clinical Trial Leader
“When the initial objectives aren’t clear or sufficiently grounded in data, the protocol needs changes later.”
CRO, Clinical Trial Leader