We are first Site Management Organization (SMO) in the Czech Republic.

WHY do we do what we do?

We offer a service to our physicians, patients and clinical study sponsors that changes the view of drug testing in the Czech Republic, mostly in outpatient care, and enables participation of a larger number of physicians and patients in clinical studies, while the quality and safety requirements are met.

HOW do we achieve this?

Our knowledge and active engagement in the study progress directly in the medical office allow participation of a greater number of physicians with various specializations in the clinical studies. We remove different types of barriers and minimize the administrative burden on the physician and their team in clinical study execution. Thus we increase the medical center capacity, quality and timeliness of data transfer. For the patient, the communication becomes easier and their questions are answered almost immediately. We innovate and are capable of managing changes. We make efforts to standardize, automate and digitalize our internal processes.

WHAT do we do?

In the medical centers of Clinical Research Center s.r.o., we make the process of development and testing of more efficacious drugs and medical devices more efficient while maintaining maximum patient safety.

Since 2016, we have been building a team of professional trained clinical study coordinators who increase the work efficiency of physicians and patient comfort by their services and knowledge.
We have formed and managed a network of selected physicians from various medical fields in order to ensure high quality elaboration and execution of clinical studies.

The cooperation of the clinical study center and a professional trained coordinator has many benefits for the physicians, the subject and the clinical trial sponsor. Together we work more efficiently.
We increase awareness of clinical studies, testing of new medication and new treatment methods. We answer the questions of both physicians and potential patients. We inform the public about studies recruiting patients.

Lucie Špatenková

We offer a service to our physicians, patients and clinical study sponsors that changes the view of drug testing in the Czech Republic, mostly in outpatient care, and enables participation of a larger number of physicians and patients in clinical studies, while the quality and safety requirements are met.

M.Sc. Lucie Špatenková
Managing Director

Člen SCRS (Society for Clinical Research Sites)

We are a member of SCRS (Society for Clinical Research Sites).

Project title: Business Development of Clinical Research Center s.r.o.
Project No.: CZ.01.2.06/0.0/0.0/16_091/0008854; the Project is co-funded by the European Union.
Project subject: Purchase of devices necessary for the work performance of CRC staff and provision of work equipment.

Cert No. 16864-QMS
ISO 9001

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