POCT diagnostics for hospitals, laboratories, and medical practices

POCT (Point-of-Care Testing) brings validated diagnostics directly to the patient — to the ward, to the doctor's office, or to the field. You get results in minutes instead of hours, without sacrificing analytical accuracy. The key difference is speed, accessibility, and compliance — the patient does not leave the doctor's office before you know the result.

Of course, gladly — the initial consultation is free and without any commitment. We'll come to you, listen to your needs, go through operational requirements, and recommend a solution that genuinely helps you. If it makes sense, we'll bring a demo device so you can try it out on the spot.

For most devices, yes — we offer a visit from an application specialist who will present the device directly at your location and leave it with you for a trial period, as agreed. Just write or call our sales contact.

We offer several models depending on your needs and testing volume — from outright purchase to long-term rental, all the way to so-called reagent rental, where we provide the device free of charge in exchange for regular reagent supply. For larger investments, we also offer installment plans or operating leasing. At the initial consultation, we'll calculate together which model will be the most economical for your practice or department.

Many POCT examinations are fully or partially covered by public health insurance under specific procedures of health insurance companies — e.g., CRP, INR, HbA1c, troponin, or urinary chemistry. Some examinations are paid out-of-pocket (premium care, occupational health checkups, aesthetic medicine, veterinary care). We're happy to walk you through specific codes and reimbursement limits at the consultation according to the type of your facility and specialty.

For stock items, within 7 business days of order; for custom configurations 4–8 weeks. We install and commission within 5 business days of delivery, including LIS/NIS connectivity and operator training.

The key is to have a device with a valid CE-IVD certificate in compliance with EU Regulation 2017/746 (IVDR) and its registration in the SÚKL Medical Device Registry. Additionally, you need an established system of internal and external quality control, trained operators with manufacturer's certification, and documented records of results and reagent batches. We help with all of it — from administration through SOP setup to device registration in the medical device system.

Yes. Every installation is accompanied by initial on-site operator training. For hospitals and the POCT program, we also offer regular recertifications, e-learning modules, and maintenance of training records in the audit trail.

Yes. We operate our own authorized service with a response time of 48 hours on weekdays throughout the entire Czech Republic and Slovakia. The contract includes regular calibrations, preventive inspections, and the supply of calibration materials and QC controls. As part of our POCT management, we also provide an external QC program.

Yes. We exclusively supply in vitro diagnostic medical devices with valid CE-IVDR certification (Regulation EU 2017/746) and notification in SÚKL (CZ) and ŠÚKL (SK). For each device and reagent, we provide a CE Declaration of Conformity, instructions in Czech, and documents for internal audits and external inspections (NASKL, SAK).

Yes — we help clients communicate new services to patients, whether it's preventive packages, seasonal campaigns (respiratory season, allergies, vitamins), or paid examinations. We provide graphic materials for waiting rooms, social media, and websites, and prepare joint information campaigns. The goal is for your investment in POCT to pay back as quickly as possible and for patients to perceive the added value of your care.

Yes — we have experience implementing POCT across entire hospitals and clinic networks. Together we'll design which parameters make sense in the emergency department, ICU, internal medicine, pediatrics, or sample collection room, and align the solution so that it's economically and operationally consistent. This includes staff training across departments and setting up unified quality control methodology.

Centralized management of all POCT devices across departments, LIS/NIS connectivity, QC oversight, user access management, training, and documentation for ISO 15189 and ISO 22870 accreditations. We will tailor the package to the size and structure of your facility.

Devices can be connected through POCT middleware, which enables remote monitoring, central configuration, reagent distribution, and result transmission directly to the hospital (HIS) or laboratory (LIS) information system. A lab technician or POCT coordinator has a single-place overview of the status of all devices, measurement quality, and consumption across departments. This significantly reduces administrative burden and increases patient safety thanks to full traceability of results.