Life Sciences evidence.
Delivered in days.

Kirha partners with HEOR, CRO and Medical Devices to automate their most critical workflows. Rigorously, at pace.

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CureetyPubMedClinicalTrials.govEMAEMANICEHASEpistemonikos
Use Cases

Three critical workflows.
Accelerated.

Systematic Literature Review

A traditional SLR ties up a team for months and hundreds of hours on screening alone. Our AI agents process abstracts in parallel, overnight, and deliver a first structured report within 72 hours.

Full PRISMA-compliant output. Audit trail included. Ready for regulatory submission.

95%
time saved
60K+
abstracts processed

SDTM Mapping

CDISC SDTM mapping consumes weeks of senior data manager time. Our AI agents read your raw study data, proposes domain mappings, generate SAS programs, validate against CDISC standards before producing submission-ready datasets.

Patient Data never leaves our regulated infrastructure. Every annotation decision is logged. Every derivation is traceable and explainable.

80%
cost reduction
95%
CDISC compliant
sdtm_dm_mapping.sas
1/* ─── SDTM Mapping: DM Domain ─── */
2 
3libname sdtm "/data/study_XR401/sdtm";
4libname raw "/data/study_XR401/raw";
5 
6%macro map_dm(study=, cutoff=);
7 
8 proc sql;
9 create table work.dm_mapped as
10 select
11 a.SUBJID as USUBJID,
12 "DM" as DOMAIN,
13 a.SITEID as SITEID,
14 a.BRTHDTC as BRTHDTC,
15 input(a.AGE, best.) as AGE,
16 a.SEX as SEX,
17 a.RACE as RACE,
18 a.ETHNIC as ETHNIC,
19 a.ARMCD as ARMCD,
20 a.ARM as ARM,
21 a.RFSTDTC as RFSTDTC,
22 a.RFENDTC as RFENDTC,
23 b.COUNTRY as COUNTRY,
24 "INFORMED CONSENT" as DSDECOD
25 from raw.demographics a
26 left join raw.site_ref b
27 on a.SITEID = b.SITEID
28 where a.RFSTDTC <= "&cutoff."d
29 order by USUBJID;
30 quit;
31 
32 /* Apply CDISC controlled terms */
33 data sdtm.dm (label="Demographics");
34 set work.dm_mapped;
35 attrib STUDYID length=$20 label="Study ID";
36 attrib DOMAIN length=$2 label="Domain";
37 attrib USUBJID length=$40 label="Unique Subject ID";
38 attrib AGE length=8 label="Age";
39 STUDYID = "&study.";
40 run;
41 
42 proc contents data=sdtm.dm varnum;
43 run;
44 
45%mend map_dm;
46 
47%map_dm(study=XR401, cutoff=2024-06-30);

Aligned with

ICH E9ICH E9International Council for Harmonisation
FDAU.S. Food & Drug Administration
EMAEMAEuropean Medicines Agency
TransCelerateTransCelerateTransCelerate BioPharma

Statistical Analysis Plan

From protocol to draft SAP in hours. Upload your protocol and automatically extract endpoints, populations, and analysis methods, structured into a version-controlled SAP shell aligned with ICH E9 and TransCelerate templates, ready for biostatistician review.

3h
draft SAP delivered
ICH E9
compliant

A workflow that doesn't fit in boxes?

Some of the problems we solve don't have a name yet. If you have a recurring, time-consuming task in your clinical or regulatory workflow, we can build an agent for it.

Tell us the task. We'll tell you if it's automatable.

Custom AI workflow automation
Client case · Cureety

3500+ clinicians
augmented

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

25+ sources
450+ million records
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.

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