We coordinate

Clinical Trial
National Centre

providing a consistent national approach for commissioners of studies
and offering a comprehensive and targeted service.

Clinical Trial National Centre

or CTNC, provides research, methodological, technical and operational support for clinical research projects. CTNC’s team of experts offers both comprehensive and targeted services – from expert consultation to training – that facilitate the implementation of clinical trials and clinical research projects involving pharmaceuticals, diagnostic methods and medical devices. All activities are carried out in accordance with applicable EU and Czech legislation and Good Clinical Practice (GCP) principles.

National Clinical Trials Centre (CTNC) methodologically manages and coordinates Local CT HUBs (CTUs)which directly support the implementation of clinical trials in all 18 teaching hospitals. It also acts as a central national contact point for all those who wish to conduct clinical research in the Czech Republic. It provides a one-stop-shop service designed to support the rapid, efficient and high-quality implementation of research projects.

Services provided

Commissioning and project management of the study

Preparation of study documentation

Medical writer and consultant

Processing the study with the regulatory authority

Processing of the study by the ethics committee

pharmacovigilance

monitoring

Local CT HUBs

is a network of clinical sites collaborating on non-commercial clinical trials, which currently includes 18 institutions in the Czech Republic.

Local CTU HUBs (CTU) is involved in the planning and implementation of non-commercial clinical trials. It provides activities related to direct access to patients (trial subjects) – ensuring optimal recruitment of subjects for clinical trials. It also participates in the solution of specific activities of clinical trials projects implemented with the support of VVI CZECRIN through the Clinical Research Coordinator, thus fulfilling the basic need for researchers in the Czech Republic.

Clinical trials

non-commercial type form an important part of clinical research in the Czech Republic. Thanks to the CZECRIN infrastructure and the network of Local CTU HUBs, research teams from different healthcare institutions can systematically collaborate, share expertise and conduct clinical trials according to international standards.

Below, you will find an overview of studies that have been created or are ongoing with the support of our infrastructure – from protocol development and regulatory documentation to patient recruitment, center coordination and quality management. For each study, we list its field, phase, design type, and current status so that you can easily get an overview of its progress.

VIII National Clinical Trials Day: development of clinical trials in the Czech Republic

Development of clinical trials in the Czech Republic On Wednesday 29 May 2025, the 8th National Clinical Trials Day took place in the representative premises of the Kaiserstein Palace in Prague. The event organized by the Czech...

How does treatment for gastrointestinal cancer affect the possibility of having children? Take part in an international questionnaire study

Cancer treatment saves lives, but it can also have long-term adverse effects that are less talked about - for example, the impact on the ability to have children. Many patients with cancers of the digestive tract, including oesophageal, stomach, pancreatic, liver,...

VIII National Meeting of Study Nurses and Clinical Trial Coordinators

VIII National Meeting of Study Nurses and Clinical Trial Coordinators We are currently preparing the 8th national meeting of study nurses and clinical trial coordinators, which is organized by the Masaryk Institute of Oncology in collaboration with the Faculty of...

CZECRIN Scientific Annual Conference 2023

BLOCK I – INTERNATIONAL COOPERATIONRegina DemlováCREATICPresentationJacques DemotesDecentralized Clinical TrialsPresentationJon Salmanton GarciaVaccelerate – Voluntary Register update, development and new research activitiesPresentationMarta Del AlamoERA 4...

6th National Meeting of Study Nurses and Clinical Trial Coordinators

The conference was held on 7 September 2023 at the Faculty of Medicine of Masaryk University in Brno. The main organizers are the Masaryk Memorial Cancer Institute, the CZECRIN research infrastructure, and the PharmAround Foundation.Block I – Clinical Trials for the...

5th National Meeting of Study Nurses and Clinical Trial Coordinators

The 5th National Meeting of Study Nurses and Clinical Trial Coordinators, organized by the Masaryk Memorial Cancer Institute in cooperation with the Faculty of Medicine, Masaryk University, the CZECRIN research infrastructure, and the PharmAround Foundation.Block I:...

CZECRIN Annual Scientific Conference 2022

Session I: Discipline-based networks for clinical trialsRegina DemlovaIntroductory word on the development of CZECRIN with a focus on DONetsPresentation | LectureIrena DoležalováDONet: EPIPresentation | LectureFilip TrbusekAcademic KH at the NÚDZPresentation |...

CZECRIN Annual Scientific Conference 2021

Session I: Discipline-based networks for clinical trialsRegina DemlovaThe concept of "CZECRIN disease-oriented networks" at national levelLectureRobert MikulíkPresentation of the national ict research network STROCZECHLectureZuzana MotovskáPresentation of the national...

Science Talk: “The Story of Drugs – The Biggest Failures That Impacted Drug Development”

Science Talk: "The Story of Drugs - The Biggest Failures That Impacted Drug Development" ICRCAcademy in cooperation with CZECRIN Academy presents SCIENCE TALK with Lenka Součková, PharmD, Ph.D. On Science Talk, you will learn about the major failures that have...

Do you need a methodological consultation?

Just fill in the form and we will suggest the most suitable service or combination of services for your project.

Mandatory consent

Do you need a methodological consultation?

Just fill in the form and we will suggest the most suitable service or combination of services for your project.

Mandatory consent