Notice: Function _load_textdomain_just_in_time was called incorrectly. Translation loading for the post-smtp domain was triggered too early. This is usually an indicator for some code in the plugin or theme running too early. Translations should be loaded at the init action or later. Please see Debugging in WordPress for more information. (This message was added in version 6.7.0.) in /var/www/cwbk.umed.pl/public_html/wp-includes/functions.php on line 6114
Cooperation scope

Cooperation scope

We provide comprehensive support in planning, coordinating and managing single or multi-centre clinical trials and pre-clinical studies with a use of the University facilities and strong academic support.

Our practical knowledge comes from the project management experience – at every stage of its cycle – starting from the idea and initial concept, through the implementation, to the preparation of the Clinical Study final Report.


For the Investigator

We would like to encourage all Investigators, who have an idea for a clinical trial and are looking for support in its planning, management and implementation, to get in touch with our unit.

The earlier we start working together, the more time we will have to develop a successful Project together.

At the initial planning stage, we can provide assistance with:

  • Checking available funding sources and selecting the best one for the project;
  • Verifying the project documentation from the formal point of view;
  • Finding strategic partners for the project;
  • Verifying project feasibility;
  • Constructing the budget required for the project to be achievable;
  • Preparing, negotiating and processing agreements required for the implementation of the clinical trial;
  • Submission of the application for funding.

Once funding is obtained, we can offer support in the implementation of the Project, in particular by dedicating a team of specialists to coordinate and monitor the ongoing Clinical Trial which can provide:

  • Legal assistance;
  • Monitoring and auditing;
  • Pharmacovigilance;
  • Administrative coordination.

For the Sponsor

CRO support

If you are planning to launch a new clinical trial project or if you need support in the implementation of an ongoing project, we can help you carry out the necessary activities, including but not limited to the below:

  • Verify the project and study documentation from the formal perspective;
  • Prepare, negotiate and process agreements required for the implementation of the clinical trial;
  • Prepare the statistical analysis plan;
  • Prepare required formal documentation to the Competent Authorities (URPL and Bioethics Committee);
  • Legal assistance;
  • Monitoring and auditing;
  • Pharmacovigilance;
  • Financial oversight of project implementation;

Study Site

We can provide support in the clinical trials implementation by providing Study Site at one of the 3 teaching hospitals:

Within their scope, we have access to a full range of medical services provided in more than 80 clinics. In total, they have 1,800 hospital beds, employ over 3 100 doctors and the approximate number of patients treated there annually is close to 114 000.

In addition, we are constantly developing a network of partnerships with the primary care facilities (POZ), which provides an additional source of a wide range of patients.

Early Phase Site

Cooperation scope
share