WHY do we do what we do?

New drug development could never work without active engagement of volunteers – patients. We bring new possibilities of treatment and diagnostics to our patients. For a large portion of the patients, participation in a study as such is a unique opportunity to get a newly developed and not yet available drug. The majority of potential patients are not aware of these options or they have many concerns, prejudices or questions.

For this reason, we increase awareness of the way of testing of new drugs and new treatment options, to dispel any concerns and fears originating from lack of knowledge and prejudice. We believe that eventually this will make new types of treatment available to a larger number of patients already during the drug testing phase and accelerate their approval for the general public and those who need them. Your voluntary participation thus helps in development of new drugs for many other people as well.

HOW do we achieve this?

Communication, access to information and mutual trust are the key to success here.

We try to explain the principle of a particular study in comprehensive and simple terms both to volunteers and those who opt for study participation as one of the few possibilities to alleviate their problems, we assist in scheduling your sessions, we protect your safety.

We emphasize the key aspects of participation in the study, mostly its voluntary nature. Each patient has the opportunity to ask their attending physician or a member of the study team any question concerning the clinical trial. The patient is also entitled to withdraw their consent to the clinical study participation any time.

WHAT do we do?

Through general public education, we introduce the basic facts and rules of drug testing to patients of our centers as well as to the general public. New studies open for patient recruitment are regularly announced on our website and communicated through the network of our physicians and medical centers.

We will provide potential patients interested in clinical study participation with a contact to a physician and arrange a meeting. If the patient decides to participate in the study, we assist them throughout the process, we help answer any questions and arrange patient sessions in accordance with the study requirements.

Our team – the physician and coordinator of Clinical Research Center are an experienced center for clinical study execution. Phases II, III, IV of clinical studies are executed at a high professional and expert level in accordance with the study protocol, good clinical practice (GCP), local and European laws and regulations. All coordinators and physicians of Clinical Research Center have been duly trained and certified.

CRC Home Care offers sufficient resources and infrastructure to provide a reliable support of clinical trials with home care visits, in line with the approved protocol and local regulations.