Grow lifetime value through personalized, continuous care

We currently provide interpretation for 100+ commonly ordered laboratory tests.

We continuously expand the list of supported tests and parameters based on our partners’ needs and patient demand.

The complete and regularly updated list of covered tests is available here.

LabTest Checker by Labplus® is a clinically validated Class I medical device built on a fundamental principle: effective lab test interpretation requires medical context.

While some solutions rely on color-coding abnormal values or providing generic information, we collect comprehensive medical context through a questionnaire before interpreting results—including diagnosed diseases, symptoms, medications, supplements, and risk factors.

This approach ensures interpretations account for each patient’s individual situation. With this complete picture, we deliver personalized recommendations and next steps.

Yes, our medical software is fully compliant with all relevant data protection and medical device regulations within the European Union.

• MDR compliance – our software is registered as a Class I medical device under the EU Medical Device Regulation (MDR) and holds the CE marking, confirming its compliance with EU safety and quality standards.
• GDPR compliance – we strictly adhere to the General Data Protection Regulation (GDPR), ensuring secure data handling, transparent privacy practices, and full respect for patient rights.

Our commitment to accuracy and performance is unwavering, with validation processes specifically tailored to the regulatory environments and clinical standards of each market we serve.

• Regulatory compliance – we meet all relevant medical device regulations, such as obtaining the CE marking in the EU.
• Country-specific adaptations – we carefully customize our model for each new market, ensuring full alignment with local regulations and standards.
• Local clinical standards – our interpretations are validated against the diagnostic and treatment guidelines practiced in each region.
• Continuous monitoring and improvement – beyond initial validation, we actively monitor real-world data from each market to identify opportunities for refinement, ensuring sustained optimal performance as clinical practices evolve.

Yes. We offer fast, secure, and seamless integration with your existing LIS — typically completed within 8 days.

1. We use WebAPI technology to embed an iframe directly into your existing patient portal, ensuring a smooth and consistent user experience.
2. We will need a dictionary of test names and parameters to complete the integration.
3. Other than that, all we require are raw lab test results. A secure connection is established to transmit anonymized, de-identified data upon patient request.

What are the benefits?

• Quick onboarding with minimal IT effort on your side.
• Ongoing technical support, whether you use your own LIS or a third-party system.
• No disruption to your existing workflows.
• Enhanced patient experience and a clear competitive advantage through value-added services.

View and download the Technical Onboarding Brief.

The bootstrapping meeting is an initial consultation where we discuss all aspects of launching LabTest Checker by Labplus® in your system. The meeting can be conducted online and typically lasts no more than 2 hours.

• During the session, we’ll cover product and technology topics, explain the patient journey, discuss technical integration aspects, define the scope of work needed for implementation, and review the work framework.
• We recommend having both product and technology team representatives present. From our side, the meeting will be led by Jakub Górowski (Chief Technology Officer) and Szczepan Czyczerski (Chief Growth Officer).
• To ensure the meeting is productive, we ask that IT department members familiarize themselves with the materials we will provide you with via e-mail.

Our interpretation is shaped by each patient’s unique health profile, collected through a medical questionnaire.

How it works:

• Dynamic questionnaire adapts in real time based on patient responses
• Covers essential health factors, i.e., diagnosed illnesses, symptoms, medications, supplements, risk factors
• Takes 2–5 minutes to complete
• Optional prevention & symptom analysis module available.

This medical context directly informs urgency classification, result interpretation, and test recommendations—ensuring clinically relevant guidance for each patient.

Our clinical validation demonstrates exceptional performance in patient safety and practical healthcare delivery. What matters most is that we never miss critical conditions. 

The Medical University of Silesia conducted the clinical trial in collaboration with a University Hospital, and the study compared the triage accuracy of LabTest Checker by Labplus® with the expertise of experienced physicians.

Key results:

• 100% sensitivity for emergency cases – every critical condition requiring immediate medical attention is identified.
• 92.3% sensitivity for urgent cases – nearly all conditions requiring prompt medical consultation are flagged.
• 82.9% accuracy in identifying underlying conditions.
• 74.3% overall interpretation accuracy – reflects a conservative approach that prioritizes safety. I.e., for routine cases, our system may recommend follow-up even when a physician might not.

Clinical validation results are published in JMIR Medical Informatics (2024;12:e57162). The summary can be found here.

We take patient privacy very seriously and do not collect any personally identifiable information to perform the interpretation.

• Our interpretation process uses only de-identified data: lab test parameters, results, reference ranges, and relevant test-specific details.
• During the interpretation process, we do not receive names, dates of birth, or any other information that could identify an individual.
• An email address is collected only if a patient chooses to contact our medical team — and it is used exclusively to respond to their inquiry.
• Anonymized data is handled with utmost care: we use end-to-end encryption, strict access controls, and secure transmission protocols at every step.

Read Privacy Policy Part B to learn more about the process.

As a medical entity providing a medical service, we take full responsibility for the accuracy and safety of our interpretations. 

• We follow strict medical device standards. In the unlikely event of errors or misinterpretations, we assume full liability — our partners bear no responsibility.
• We maintain a comprehensive insurance policy in the event of any adverse outcomes related to our interpretations.
• Our terms of use are clearly outlined in the user’s manual (available here), in accordance with CE regulations. Patients are fully informed about the nature of our service and any potential limitations.
• We implement strict quality controls, including physician oversight, to minimize the risk of errors. Our clinical validation studies demonstrate the high reliability of our interpretations.

We proactively analyze all cases to continuously refine our models and enhance the accuracy of our service.