Clinical Trials Department
Clinical studies are research investigations conducted to test new drugs, medical devices, or to evaluate innovative therapeutic and diagnostic procedures. These studies involve real patients with specific medical conditions relevant to the research focus. All clinical trials are conducted in compliance with internationally recognized ethical and scientific principles and are subject to rigorous legal and regulatory oversight. At every stage, patient safety, rights, and well-being remain paramount.
Martin University Hospital ranks among the excellent medical and academic institutions of international significance. Our experienced specialists conduct numerous clinical trials, primarily in phases II-IV, covering a broad range of therapeutic indications across various therapeutic areas, including pneumonology, gastroenterology, cardiology, hemato-oncology, nephrology, urology, dermatology, paediatrics, neonatology, oncology, neurology, radiology, and surgery.
We actively collaborate with prestigious international research networks such as SLOVACRIN, H2020 – TENSION, Horizon Europe – THCS, and the Digital Europe Programme – TEFs. Martin university hospital is registered in the OMS (Organization Management Services) system of the European Medicines Agency (ORG ID: ORG-100041101). We create a dynamic and innovative research environment and represent a trusted partner for leading pharmaceutical and biotech companies, medical device manufacturers.
We take pride in our contribution to medical innovation, bringing our patients access to the most advanced and state of the art treatment and diagnostic options.
The Clinical Trials Department is a centralized service unit of the Martin University Hospital, primarily dedicated to coordinating research personnel throughout the planning, start-up, and execution of clinical trials. The department provides administrative and organizational support, allowing researchers to focus their time, energy, and expertise on clinical and scientific work. Our objective is to conduct high-quality clinical trials that comply with national legislation and adhere to stringent internationally recognized standards (e.g., ICH-GCP), ensuring the protection of study participants' rights, safety, and well-being while maintaining the integrity of research outcomes.
If interested in collaboration on clinical trials, please contact us for further information at:
+421 905 231194