Laboratory Management
Redefined for India.

NHA’s own guidance and standards like HL7/FHIR encourage instrument interfaces for accurate, traceable results. Cliniqwise can integrate via standard protocols or vendor APIs so worklists go from LIS to auto‑analyzers and results return automatically, eliminating manual entry errors and speeding up report release.

NABL 112 expects detailed audit trails for data entry, result changes, instrument interfacing, and report release. Cliniqwise logs user actions, timestamps, and pre‑/post‑validation values, and supports periodic LIS verification, which laboratories must demonstrate during NABL and ISO‑15189 assessments.

Best‑practice LIS workflows separate data entry, verification, and authorisation steps. In Cliniqwise, technicians verify raw values against QC, while pathologists review flagged results and authorise final reports, ensuring a clear chain of responsibility for each test.

Many Indian labs now share reports securely via links in SMS or WhatsApp alongside traditional printouts. Cliniqwise can generate password‑protected PDFs and URLs, making it easy for patients and consultants to access reports without waiting at counters, while logs track each access for confidentiality.

Yes—labs need documentation on QC, calibrations, equipment lists, non‑conformities, and corrective actions alongside patient reports. Cliniqwise can store and index these records by date, instrument, and test, making it easier to produce evidence during NABL audits and internal quality reviews.

Integrated LIS‑HMS setups push validated results to the patient’s EMR and, where enabled, into ABDM FHIR bundles for ABHA‑linked sharing. This ensures clinicians see up‑to‑date results in context and patients can access their lab history through national digital health platforms.