SmartOnco
Purpose-built for cancer care: diagnosis, MDT collaboration, evidence-based treatment protocols, chemotherapy administration, and clinical trials — in one HL7 FHIR-compliant platform.
Digital Excellence for Every Stage of the Cancer Care Journey
SmartOnco is Absolute Solutions' purpose-built oncology management system, digitising every aspect of cancer care from initial diagnosis and multidisciplinary team collaboration through chemotherapy administration, radiation oncology, and clinical trials management.
Built to international standards — HL7 FHIR R4, ICD-10-CM, SNOMED CT, and DICOM — SmartOnco ensures seamless interoperability with hospital information systems and national cancer registries.
SmartOnco
Structured oncology records. NCCN/ESMO protocol library. Bedside barcode verification before chemotherapy. CTCAE toxicity monitoring in real time.
Key Features
Every clinical and operational capability needed to run a world-class oncology service.
Patient Oncology Profile
Rich, structured oncology records from first consultation to survivorship.
Treatment Planning & Protocols
Evidence-based treatment planning with automated dose calculation.
Chemotherapy Administration
Closed-loop safety at the bedside — every administration verified.
Radiation Oncology
Integrated radiation treatment plan management and fraction tracking.
Clinical Trials Management
Full trial lifecycle from protocol setup to adverse event reporting.
Oncology Analytics
Outcome tracking, survival analysis, and quality improvement dashboards.
Healthcare Standards Supported
SmartOnco is built to the same international standards used by leading cancer centres globally.
| Standard / Framework | Compliance Level |
|---|---|
| HL7 FHIR R4 | Full bidirectional interoperability — read/write APIs |
| ICD-10-CM (Oncology) | Integrated diagnosis coding with ICD-O-3 morphology |
| SNOMED CT | Clinical terminology for all diagnoses, procedures, and findings |
| DICOM / DICOM-RT | Medical imaging and radiation treatment plan integration |
| CDISC ODM | Clinical trial data export for sponsor and IRB submission |
| HIPAA / PDPA | Patient privacy and data security compliance |
| DRAP Regulations | Drug registration and pharmacovigilance compliance |
Clinical Module Detail
The clinical depth that sets SmartOnco apart from generic EMR systems.
Multidisciplinary Team (MDT)
- Case registration and agenda management for tumour boards
- Structured MDT discussion documentation template
- Consensus treatment decision recording with participant names
- MDT outcome letter generation for GP and patient
- Follow-up action tracking and next review scheduling
Chemotherapy Safety
- Two-pharmacist sign-off on chemotherapy preparation
- Five-point patient ID verification before administration
- Weight-based dose recalculation on each cycle
- Cumulative dose tracking for dose-limiting toxicities
- Chemotherapy preparation label generation with barcode
Genomics & Precision Medicine
- Next Generation Sequencing (NGS) result import and display
- Targeted therapy recommendation based on mutation profile
- Biomarker tracking across treatment journey
- Clinical trial eligibility matching based on genomic criteria
- Genomic report storage with version history
Clinical Trials
- Protocol configuration: inclusion / exclusion criteria
- Randomisation module for interventional trials
- Case Report Form (CRF) builder and completion tracking
- Protocol deviation recording and impact classification
- Data export in CDISC ODM XML for submission to sponsors
Business Benefits
Patient Safety
Barcode verification and drug interaction alerts eliminate dangerous chemotherapy errors.
Better Outcomes
Structured protocols and MDT collaboration drive consistent, evidence-based treatment decisions.
Research Ready
Structured data collection supports clinical research and quality improvement programmes.
Accreditation
Audit-ready documentation meets DRAP, JCI, and international oncology accreditation requirements.
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