Peacewise Consulting builds clinical-grade AI platforms for healthcare diagnostics and pharmacovigilance — where accuracy is non-negotiable. Three platforms, two patents filed, one philosophy: rigour over rhetoric.
A specialty diagnostics catalog, a lead intelligence CRM, and Dr. Gene — an AI co-pilot for referring clinicians. Unified under one platform.
Hospital-grade AI for medication safety and NABH 5th Edition compliance. Built for the Indian hospital cost envelope.
Machine-learning signal detection for adverse drug reactions. Context-aware, Indian-name friendly, and regulator-ready.
SpectraDx is three products under one brand. A patient-facing booking platform with a specialty test catalog across PCR, FISH, NGS and cytogenomics. A lead intelligence CRM that maps clinicians and hospitals across India and neighbouring regions. And Dr. Gene — an AI assistant that helps referring physicians interpret specialty results in context.
The patient booking flow, admin console and AI co-pilot are live and working together as a single diagnostics experience — designed for clinicians, ordered by patients, and built to scale with partner labs.
MedSafe turns hospital medication workflows into auditable, AI-assisted pipelines. Medication reconciliation at admission, near-miss reporting, sentinel event tracking, LASA detection, formulary governance, drug recall response, and controlled-substance audit — all aligned with NABH 5th Edition.
The platform includes a Smart Data Mapper that cleans messy clinical exports, and a European companion — MedSafe EU — built for EudraVigilance, GDPR and FHIR standards.
Adverse drug reactions are under-reported globally — and especially in India, where clinical notes arrive in free text, transliterated names, and inconsistent formats. Our ADR engine reads that reality. It cleans, normalises and clusters reactions using logic tuned to Indian patient names and prescribing patterns.
Missing a true safety signal is the only failure mode that counts. Results feed directly into regulator-ready reports for both Indian and European submission standards.
Every algorithm we ship is anchored to peer-reviewed evidence, established registries, and the actual workflows of clinicians who will use it. Published medical standards and NABH — these are our north stars.
We design for the operational and economic realities of Indian hospitals and labs — without compromising on regulatory compliance, auditability, or the quality standards global enterprises expect.
Indian deployments are designed with the DPDP Act and domestic data residency in mind. European deployments are built for GDPR and EU medical device regulation — the same platform, with sovereign data paths.