Software for a newborn’s first days, built by a neonatologist.

ClinicalQI Healthtech LLP makes three tools for Indian NICUs: guided resuscitation at birth, nursing documentation that produces your NABH evidence, and checked drug dosing.

NeoEnigma nurse home screen showing assigned babies, checklists and tasks for the shift
NeoRes screen guiding ventilation at 40 breaths a minute with live heart rate, SpO2 and temperature

Three products, from birth to discharge

Each one covers a stage of the newborn’s journey and is built only for neonates, never adapted from adult care.

In development. CDSCO licensing in progress; not yet for sale.

NeoRes oxygen titration screen with live heart rate and SpO2

At birth

NeoRes

Clinical decision support for neonatal resuscitation. It reads live heart rate, SpO₂ and temperature and speaks each step aloud.

  • Aligned with IAP NRP STG 2022 and AHA/AAP NRP 9th Edition (2025)
  • Fully functional offline; no patient data leaves the device
  • Voice guidance in English, Hindi, Marathi, Telugu and Tamil
  • Post-resuscitation documentation and handover summary
More about NeoRes
NeoEnigma nurse dashboard with babies, checklists and unit observations

In the NICU

NeoEnigma

A nursing workflow and quality system. Nurses document care once at the bedside; registers, KPIs and the NABH evidence pack derive from it.

  • 17 bedside forms, 26 auto-derived registers, 24 nursing-sensitive KPIs
  • One-click NABH evidence pack, designed around NABH 6th Edition
  • Tamper-evident audit trail with named attribution
  • ABHA capture at registration (ABDM Milestone 1)
More about NeoEnigma
What NeoRx calculates: antibiotics and drugs, infusions, IVF and TPN, electrolyte correction, the all-orders sheet and error reporting

Every prescription

NeoRx

Neonatal medication safety. NeoFax/NNF-based dosing adjusted for weight, gestational age, day of life and renal function.

  • 56+ neonatal drugs and 14+ continuous infusions
  • IVF and TPN calculation with fluid-overload prevention
  • Sodium, potassium and calcium correction calculators
  • Print-ready order sheets, reviewed and signed by the physician
More about NeoRx

ClinicalQI products are decision support and documentation tools. They support, and do not replace, the clinical judgement of trained healthcare providers, and all orders require physician review, verification and signature before administration. Feature lists reflect what each product is committed to at launch. More software across the newborn’s journey is on the way.

Better outcomes for every newborn, from birth through the NICU to home

ClinicalQI exists to improve neonatal outcomes at every stage of the newborn’s journey. That starts with the people at the bedside: we streamline every nursing task so that nurses spend their time with babies rather than buried in documentation, manual or digital.

Every solution is custom-made for neonates and NICUs, never adapted from adult care, and built by Dr. Harshal Khade, a practising neonatologist who lives these workflows every day.

Because tools alone don’t change outcomes, we collaborate with Acuity Academy to train and upskill nursing teams, so the people grow more capable along with the process.

BirthProtocol-perfect resuscitation in the first golden minutes.NeoRes
NICUStreamlined nursing workflow, NABH evidence and medication safety.NeoEnigma and NeoRx
HomeDischarge and beyond. The journey doesn’t end at the NICU door.More software on the way

How we build clinical software

Guideline-driven, cross-validated

Clinical content is derived from published Indian guidelines (NNF Clinical Practice Guidelines, AIIMS protocols, IAP) and international references such as NeoFax and the AHA/AAP NRP, cross-validated across sources and reviewed by a Neonatologist before release.

Physician in the loop, always

Every product is designed as decision support or documentation. Physicians review, verify and sign clinical outputs; nurses document real care, not audit forms. Software never replaces clinical judgment.

Evidence you can trust

Append-only registers, hash-chained audit trails and named attribution on every entry. What a surveyor, auditor or court sees is what actually happened at the bedside. There is no manual write path and no retrospective editing.

Regulatory discipline by design

We know exactly where the medical-device line sits and we engineer to it: deliberate capture-and-display boundaries where appropriate, formal SaMD development where warranted, and a firewall between the two.

The standards we build to, and where each product stands

How every product is built

Quality at ClinicalQI is a company-wide discipline, not a per-product afterthought. Every product is developed under quality-management and software-lifecycle processes aligned to international medical-software standards, with risk management and usability engineering built into the process. Every piece of clinical content is reviewed by a Neonatologist before release.

  • ISO 13485
  • IEC 62304
  • ISO 14971
  • IEC 62366-1
  • IEC 82304-1

Patient safety leads every design decision: physicians review, verify and sign clinical outputs, and each product is engineered with a clear view of where the medical-device line sits. Where a product falls within the scope of India’s Medical Device Rules 2017, it will reach the market only with the appropriate CDSCO licence; the regulatory pathways are in progress.

Data protection & integrity

All infrastructure is hosted in India on AWS (Mumbai region), with per-facility isolation, pseudonymised analytics and no PII egress, in an architecture aligned to the Digital Personal Data Protection Act, 2023.

Clinical records are engineered to be tamper-evident: append-only storage, cryptographically hash-chained audit trails, and named attribution on every entry. What was recorded is what happened; data cannot be silently altered or deleted. Every system is built for the realities of Indian hospital networks.

Learn: notes from the NICU

See all notes
Dr. Harshal Khade, founder of ClinicalQI

Founded by a practising neonatologist

ClinicalQI Healthtech LLP was founded in Nagpur by Dr. Harshal Khade, a practising neonatologist building the tools he wished his own unit had: software shaped by real NICU workflow rather than adapted to it afterwards. The company is incubated at BioNEST DMIHER, Wardha, a DBT-BIRAC supported bioincubator.

  • IAP Neonatology Fellowship
  • Over nine years in NICU, tele-ICU and paediatric care
  • 7 peer-reviewed publications
  • DPIIT-recognised startup

Dr. Harshal Khade, Founder & Designated Partner · Neonatologist, Clinical Lead
Dr. Kalyani Besekar (Khade), Co-founder & Designated Partner

Read Dr. Khade’s profile

Partners and ecosystem

Hardware & distribution

Acuity Neocare Pvt. Ltd.

Lucknow-based manufacturer of the neonatal monitoring hardware our software integrates with. Acuity Neocare takes the combined solution to hospitals.

Training

Acuity Academy

CAPA and quality-workflow training for nursing teams, completing the ClinicalQI quality ecosystem.

Incubation

BioNEST DMIHER, Wardha

A DBT-BIRAC supported bioincubator hosting ClinicalQI's early-stage development.

Tell us what your unit needs

We welcome suggestions about our software, and requirements from clinicians. If your hospital needs a tool that doesn’t exist yet, describe the problem and we will explore building it. Partnership enquiries from hospitals, institutions and industry are equally welcome.

Innovation cohort

Be among the first. Hospitals that join our initial innovation cohort receive ClinicalQI software at 50% off launch pricing, along with a direct line to the clinical team shaping each product.

Register interest

Talk to us

For a demo of any of our software, suggestions, partnership enquiries or anything else, write to us, call, or use the form.

Email

admin@clinicalqi.com

clinicalqihealthtech@gmail.com

Phone

+91 77386 44009

Address

Mangala Polyclinic, Aaradhana Nagar,
Plot No 157-158, Shideshwar Nagar,
Dighori, Nagpur, Maharashtra 440009