RadiTech Sh.p.k. is a specialized medical device engineering company providing end-to-end services across sales, installation, calibration, quality assurance, and regulatory compliance for radiological and oncology equipment — supporting hospitals and cancer centers throughout Albania and the wider region.
RadiTech Sh.p.k. is a registered limited liability company based in Tirana, Albania, founded on February 16, 2024. We are an independent, vendor-neutral medical device engineering company specializing in radiation technology — from ionizing systems used in cancer treatment to non-ionizing diagnostic and therapeutic equipment.
Our team brings together over 11 years of combined hands-on experience in biomedical engineering, clinical medical physics, radiation safety, and healthcare informatics. We work directly with hospitals, oncology centers, radiology departments, and research institutions to ensure their equipment operates safely, accurately, and in full compliance with applicable technical and regulatory standards.
Because we are manufacturer-independent, we are free to provide unbiased assessments, multi-vendor servicing, and technology-neutral recommendations — always prioritizing what is right for your facility and your patients, not what benefits a single manufacturer.
Deliver engineering solutions that protect patient safety, extend equipment life, and empower healthcare professionals with reliable, compliant radiation technology.
Client-centered, technically rigorous, and fully transparent — each engagement is scoped to your facility's specific clinical needs, equipment landscape, and regulatory environment.
Integrity and professionalism underpin everything we do. We communicate clearly, document thoroughly, and hold ourselves to the same standards we help our clients meet.
Based in Albania and serving healthcare facilities across the broader Western Balkans region, we understand the local regulatory environment and logistical challenges that larger international firms often overlook.
Linear accelerators, CT simulators, brachytherapy units, diagnostic X-ray, and fluoroscopy systems
MRI, diagnostic and therapeutic ultrasound, laser-based devices, and RF medical equipment
OIS deployment, configuration, user training, and technical support across multi-vendor clinical environments
Absolute dose measurement, output constancy checks, beam data acquisition, and traceable calibration programs
Facility radiation surveys, shielding design review, radiation protection program development, and personnel dosimetry management
Custom clinical applications, medical device data integration, and workflow automation for radiology and oncology departments
From initial procurement and commissioning through to long-term quality assurance and regulatory compliance — RadiTech provides the full engineering lifecycle for your radiation oncology and radiology department, with a single accountable point of contact throughout.
We source, import, export, and supply medical and radiological devices from internationally certified manufacturers to healthcare facilities across the region. Our procurement process includes technical evaluation, regulatory documentation review, customs clearance coordination, and delivery logistics — ensuring your equipment arrives complete, certified, and ready for commissioning.
Our engineers perform full equipment installation and site commissioning for new systems, as well as scheduled preventive maintenance and corrective repair for existing installations. All work is performed according to manufacturer technical documentation, applicable international standards, and the specific operating conditions of your facility — minimizing downtime and protecting your investment.
We provide independent radiation safety consulting services to help facilities meet their legal obligations and protect staff, patients, and the public. Services include radiation surveys, area monitoring, shielding calculations and design review, personal dosimetry program management, radiation protection program audits, and preparation for regulatory inspections.
Accurate, reproducible measurements are fundamental to safe radiation therapy and diagnostics. We design and implement traceable calibration protocols and comprehensive quality assurance programs for ionizing and non-ionizing radiation systems — covering output consistency, geometric accuracy, imaging performance, and mechanical integrity, in line with internationally accepted clinical standards.
We implement, configure, and support oncology information systems and radiology information platforms, and develop custom clinical software and workflow tools tailored to your department's needs. We also provide full hardware-to-software integration services, connecting treatment systems, imaging devices, and clinical networks into a unified, interoperable environment.
Effective operation of complex medical equipment requires well-trained staff and a strong compliance culture. We deliver structured training programs in radiation safety principles, device operation, quality assurance procedures, and regulatory requirements — tailored to clinicians, physicists, radiographers, and technical staff. We also assist facilities in preparing documentation and processes for regulatory submissions and inspections.
In a field where precision and trust are non-negotiable, the partner you choose matters. Here is why healthcare facilities across the region choose RadiTech.
We have no exclusive agreements with any equipment manufacturer. That means every recommendation we make is based entirely on your clinical needs, budget, and long-term operational goals — not on supplier incentives. We service and support equipment from all major manufacturers.
We are based in Albania and have direct knowledge of the local healthcare regulatory environment, procurement frameworks, and logistical landscape. We understand the practical challenges of operating advanced medical technology in the Western Balkans region — and we build that understanding into every engagement.
Our engineers and physicists apply the same technical protocols used in internationally accredited cancer centers. Calibration procedures, QA tolerances, and safety assessments are performed to internationally recognized clinical guidelines — not approximations.
From procurement and installation to ongoing maintenance and compliance, you have one dedicated team managing your equipment lifecycle. No handoffs between departments, no gaps between contracts, and no ambiguity about who is responsible for what.
Regulatory compliance is not an afterthought for us — it is built into every service we deliver. Our documentation, protocols, and service reports are designed to support your facility's regulatory submissions, internal audits, and accreditation processes from day one.
Equipment downtime in a clinical environment has direct patient impact. We prioritize rapid response for urgent service needs and work around your clinical schedule to minimize disruption. Our team is reachable seven days a week during extended business hours.
The following examples reflect the types of engagements we undertake for healthcare facilities in the region. Client details are shared with permission only. Contact us to discuss how we can support your specific project.
Full clinical commissioning of a multi-energy radiation therapy system, including absolute dose calibration, beam data acquisition, mechanical and geometric verification, imaging system QA, and development of the facility's ongoing quality assurance program. The engagement included staff training on daily, monthly, and annual QA procedures.
Independent radiation protection audit for a newly constructed radiology department prior to regulatory licensing. Scope included review of architectural shielding plans, on-site radiation surveys following equipment installation, occupancy dose assessments for adjacent areas, and preparation of the facility radiation protection program documentation for submission to the national regulatory authority.
Ongoing preventive and corrective maintenance program covering a portfolio of ionizing radiation systems across a single oncology department. Services include scheduled maintenance visits, unscheduled corrective repairs, spare parts management, performance testing, and detailed service documentation in support of the facility's internal quality system and regulatory requirements.
End-to-end implementation of an oncology information system for a radiation therapy department, including server configuration, network integration with treatment delivery and imaging systems, data migration from legacy records, workflow configuration, and comprehensive training for clinical and administrative users. The project also included development of custom reporting tools tailored to the department's clinical workflow.
Have a project in mind? We welcome early-stage conversations about scope, feasibility, and budget.
Discuss Your Project →Every service RadiTech delivers is grounded in the applicable international regulatory frameworks that govern medical devices, radiation safety, and quality management systems. Our compliance-first approach gives clients confidence that the work we perform will stand up to regulatory scrutiny at every level.
All medical devices we supply and service are assessed against European CE marking requirements under the Medical Device Regulation (MDR 2017/745). We support clients in understanding their obligations under applicable device classifications and conformity assessment pathways.
MDR 2017/745Our quality management approach is aligned with ISO 13485, the international standard for quality management systems in the design, production, and servicing of medical devices. We apply its principles to documentation control, non-conformance management, and service process validation.
ISO 13485Radiation protection programs and dosimetry services are conducted in full alignment with IAEA Safety Standards, including the Basic Safety Standards for protection against ionizing radiation. We apply these frameworks across facility surveys, personal dosimetry, and radiation protection program development.
IAEA BSSAll software implementations and systems integration projects are delivered with full adherence to medical imaging interoperability standards and applicable patient data protection legislation, ensuring that clinical data is handled securely, consistently, and in a format that supports long-term system compatibility.
Data StandardsOur team combines certified biomedical engineers, clinical medical physicists, radiation safety specialists, and clinical software engineers — all united by a shared commitment to technical excellence and patient safety. Every team member brings direct clinical and industry experience, not just theoretical knowledge.
Senior leadership with combined expertise spanning clinical radiation technology, healthcare business development, and medical device regulatory affairs — providing strategic direction and client relationship oversight across all engagements.
Qualified biomedical engineers with direct hands-on experience in the installation, commissioning, calibration, scheduled maintenance, and corrective repair of radiological and oncology equipment across multiple device categories and manufacturers.
Qualified radiation protection experts and clinical physicists providing dosimetry measurement, safety audits, shielding assessments, regulatory compliance guidance, and staff training programs — aligned with national and international radiation protection standards.
Experienced clinical software engineers and informatics specialists delivering oncology and radiology information system implementations, custom clinical applications, and end-to-end hardware/software integration solutions across complex multi-system clinical environments.
Whether you are planning a new equipment installation, need ongoing maintenance support, require an independent radiation safety audit, or want to discuss a clinical informatics project — our team is ready to help. We offer no-obligation initial consultations and welcome early-stage enquiries at any stage of your project planning.
Rruga "Dora D'Istria", Nd.66, H.4
Tiranë 1001, Albania
Monday – Sunday: 09:00 AM – 10:00 PM
Our team will respond within one business day.