From Evidence to Compliance.In days.

AI agents for HEOR, pharmacovigilance, and clinical decision support. Source-grounded. Audit-ready.

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CureetyPubMedClinicalTrials.govEMAEMANICEHASEpistemonikos
< 5s
Cited clinical answer
real-time, source-grounded
72h
PRISMA-aligned SLR
vs. 6 weeks manual
24/7
Safety signal surveillance
ICH E2C(R2) aligned

Clinical Evidence Retrieval

Medical knowledge now doubles every 73 days. Kirha embeds it in every decision.

Real-time, source-grounded clinical search embedded inside your clinician-facing product. Every answer backed by the latest guidelines, trials, and labels, resolved in the native grammar of each source.

< 5s
cited answer
Real-time
source queries

Run where Patient Data must stay

HDS-certified in France. Sovereign cloud, on-prem or your VPC elsewhere.

kirha.agent / medical

Clinician query

Kirha · clinical agent

Olaparib, rucaparib, niraparib and talazoparib all sit in the RxNorm PARP-inhibitor class (ATC L01XK). EMA authorises Lynparza monotherapy after new hormonal agents, Akeega (niraparib + abiraterone fixed-dose) for BRCA1/2-mutant mCRPC, and talazoparib + enzalutamide when chemo is not indicated. [1]

PROfound (NEJM 2020): olaparib improved rPFS 7.4 vs. 3.6 mo (HR 0.34) in BRCA1/2/ATM-mutated disease. TALAPRO-2: talazoparib + enzalutamide benefit in the HRR-mutated cohort. FDA mandates a BRCA1/2 companion diagnostic (BRACAnalysis CDx or FoundationOne CDx) before initiation. [2]

Systematic Literature Review

PRISMA 2020-aligned reviews in days, not months.

Two independent screener agents and a judge for conflicts. Dual-reviewer methodology, automated. Queries PubMed, Cochrane, and Epistemonikos by default; bring your own key for Embase, CINAHL, or any source you need.

72h
vs. 6 weeks manual
60K+
abstracts screened

Aligned with

ICHICHE2C(R2) · E2D
FDAU.S. Food & Drug Administration
EMAEMAEuropean Medicines Agency

Pharmacovigilance

Safety signals don't wait for your next review cycle.

Kirha agents continuously watch PubMed, EudraVigilance, FAERS, and regional sources, triaged against your product portfolio and pre-assembled into PSUR/PBRER evidence sections, ready for QPPV review.

24/7
literature surveillance
ICH E2C(R2)
aligned

A workflow that doesn't fit in boxes?

Some problems don't have a name yet. Tell us the recurring task in your clinical or regulatory workflow. We'll tell you if it's automatable.

Custom AI workflow automation
Client case · Cureety

3500+ clinicians
augmented

25+
sources queried live
5 seconds
response time
60 000+ patients
monitored daily

Not sure where to start?

Book a 30-minute call. We start from your actual workflow and identify together the highest-value automation opportunity, with no commitment.