Accelerating clinical trial start-up with AI agents.
From protocol development to site selection and patient pre-screening, Kitsa connects sponsors, sites and research teams with clarity and speed.
Your clinical trial feasibility
and startup platform.
At every step of trial start-up, Kitsa combines public registries, proprietary databases, and custom-collected intelligence into decisions tailored to your protocol.
Drafts regulatory documents grounded in published guidance, historical trial data, and your sponsor library.
Scores sites against your protocol using demographics, disease prevalence, prior trial history, and capability profiles across 300K+ trial centres.
Matches patients to your criteria using de-identified EHR data, with citations back to the source record.
No black boxes. From protocol draft to site score to patient match, every output is traceable to its sources.
KScribe
regulatory authoring in days, not months.
KScribe is grounded in clinical protocols, ICH and FDA guidance, and historical study data, with retrieval over your sponsor library.
- Structured protocol and CSR generation
- ICH E6(R3) and global-guidance alignment
- Benchmark against historical trial intelligence
EGFR-Mutated Non-Small Cell Lung Cancer
KScout
AI site selection for the right clinical research sites.
KScout ranks sites for your protocol using site demographics, local disease prevalence, prior trial history by condition and sponsor, publicly available site data, and capability profiles submitted directly by sites on the Kitsa network.
- Scored investigators and sites per indication from a 300K+ site network.
- Projected first-patient-in and screen-fail rates
- Fair, evidence-based matching with full audit trail
KScreener
precision patient matching for clinical research sites.
KScreener applies your protocol criteria to EHR data at the site and returns a ranked candidate list. Every match carries a criterion-by-criterion rationale with citations back to the source record.
- De-identified at the source · HIPAA, 21 CFR Part 11
- Explainable matches with rationale per criterion
- Ships a coordinator-ready worklist each morning
From first draft to
first patient in.
Compress start-up timelines, de-risk site selection, and turn every protocol into evidence. Purpose-built for pharma and biotech clinical operations, medical affairs, and regulatory teams.
The trials worth
running, pre-matched.
Show up in front of sponsors with your real capabilities — not a paper capability statement — and let KScreener deliver a coordinator-ready candidate list each morning.
A network of the industry's most serious partners.
KScribe is available on AWS Marketplace through Tech Mahindra's Clinical Document Studio.
Audited, certified, and aligned.
SOC 2 Type II and ISO 27001 certified. HIPAA compliant. Audit reports available under NDA.