Laboratory Software Development Services

This software automates test order processing, sample routing, and test report generation and sharing. It can also provide test result interpretation, appointment scheduling, billing, inventory management, and operational analytics.

This software enforces SOP execution, captures instrument data in real time, performs compliance deviation checks, and automates lab documentation and reporting. Moreover, it can verify reagent validity, instrument calibration, sample identity, etc.

These systems keep compliance documentation and automate tracking of nonconformances and executing corrective and preventive actions. It can also cover staff training, equipment validation, and audit preparation.

These systems store regulated documents (such as SOPs, policies, validation protocols, and maintenance logs) under strict version control. It also routes documents for approval, schedules periodic reviews, and preserves audit trails for inspections.

This software (standalone or integrated into lab devices) captures analyzer data, processes and interprets it, generates test reports, and offers diagnostic insights. It can also monitor device performance and ensure compliance with regulations.

With these portals, patients can schedule appointments, pay for lab services online, view test results, and access help and information. Data is exchanged using healthcare standards to keep records consistent and up to date (FHIR APIs with USCDI alignment).

This software enables automated charge capture and patient billing, medical coding, claim submission, and denial management, with CPT and ICD-10 support and HIPAA X12 837/835 transactions for claims and remittances. It also supports real-time claim and payment tracking and offers financial performance analytics.

These systems support tracking samples, capturing analyzer output, and generating lab reports. They can also cover QA/QC, equipment maintenance, inventory and supply management, waste disposal and compliance control, staff training, and more.

This software enables collaborative experiment designing and execution, research data analysis, documenting, and reporting. It can also support sample tracking, inventory management, and equipment scheduling, and offer advanced scientific data analytics capabilities.

These laboratory informatics solutions automatically aggregate experimental data from all laboratory systems, standardize, structure, and validate it. This enables efficient search, advanced analysis, collaborative review, and easy sharing.

This software analyses aggregated laboratory data to deliver test result interpretations or identify patterns and root causes of deviation in experimental data. It can also provide suggestions on quality control, operational and financial performance optimization, and more.

These systems provide vendor-neutral connectivity for lab analyzers. They standardize analyzer outputs, post verified results to LIS/LIMS via HL7 v2, and normalize test catalogs to LOINC where applicable. They also run real-time QC and delta checks and auto-release compliant logs and reports.

This software consolidates all lab tools (instruments, LIS/LIMS, a patient portal, finance and supply chain systems, etc.) into a coordinated ecosystem that shares clean, up-to-date information. It uses standards-based interfaces (HL7 v2 and FHIR) to reduce custom point-to-point builds and optimizes workflows through consolidated data analysis.

This software supports sample barcoding and labeling, tracks samples from collection to disposal in real time, and maintains chain-of-custody records. It can also arrange courier pickups, coordinate sample routing across multiple labs, control storage and transportation temperature, and more.

This software enables real-time tracking of laboratory supplies, supports barcode or RFID scanning, and sends low-stock and expiry alerts. It can also keep compliant inventory audit trails, automate ordering, and optimize resource utilization.

Such solutions forecast lab inventory demand, automate purchasing, track deliveries, and maintain batch traceability for regulatory compliance. It can also control supplier performance and provide analytics for cost and disruption management.

We define functional priorities, integration scope, and compliance needs. Our architects design a scalable, secure system architecture and recommend modernization or consolidation strategies. Deliverables include a detailed project roadmap with phased budgets, timelines, and mitigation plans for identified technical and regulatory risks.

We deliver full-cycle development of LIS, LIMS, ELN, and other lab software, ensuring smooth integration with lab instruments, legacy tools, and external systems. All software is validated against regulatory requirements (e.g., HIPAA, CLIA, 21 CFR Part 11, Cures Act) and documented for audit-readiness.

With low-code techs like Power Apps, we can build drag-and-drop tools that let lab managers modify data intake forms and automated workflows. Additionally, low-code can be used to create adapters for mapping instrument data into the LIMS. This reduces development costs and makes the software more agile for functionality tweaks.

We handle technical issues, monitor and optimize software performance, regularly test security controls, apply patches, and update system components. We can also provide L1 support to handle simple user issues (such as technicians’ questions about LIMS use), or L2 or L3 level support to resolve queries involving technical software problems.

We fix legacy issues in existing software to enhance automation, better integrate ecosystem components, aggregate all data, and eliminate silos. When needed, we also connect the software with new instruments and services, and add new features, including analytical and automation AI modules.