Public Sector
Turn ambitious research questions into evidence-backed studies that fit your funding, resources and institutional requirements.
Research capacity
Bring relevant evidence, comparable studies and design options together around your research question, with agents doing the groundwork. Give colleagues a clear draft to review, so their time goes into shaping the science rather than assembling it.
Study feasibility
Compare recruitment needs, visits, assessments and operational burden against similar studies. Shape a design that answers the scientific question, works for participants and sites, and fits your funding and milestones.
Review & coordination
Bring investigators, statisticians and institutional specialists into the same workflow, with evidence and comments beside the relevant clauses. Keep questions, decisions and approvals connected, so what reaches ethics and institutional review is clearer and more complete.
Projected institutional targets
Projected twelve-month targets for an academic unit supporting approximately twelve protocols annually, assessed against its baseline and agreed scope.
Target time saved from grant award to a protocol ready for review
Target reduction in first-round ethics or IRB queries
Approximately 10 → 4 per protocolTarget coverage of the agreed protocol archive
Indexed in the institutional hub within twelve monthsProjections, not measured results. Actual outcomes depend on the unit’s baseline, agreed scope and execution.
Connect past protocols, evidence, institutional guidance and recorded decisions. Altrovia combines them with public trial data so each new study builds on what your institution has already learned, with access limited to authorized teams.
“The challenge is turning everything we want to investigate into a trial we can realistically fund and deliver.”
“Developing the protocol alone took more than six months.”
“From drafting the protocol to enrolling the first patient, the process took 12–18 months.”