WHY do we do what we do?

We enable participation in clinical studies to a larger number of physicians, we remove barriers and minimize the administrative burden on the physicians executing clinical studies. Together we increase the physician’s team capacity for study execution in order to make the tested medication available to the largest possible number of patients in the center.

With our support and knowledge, even medical teams that doubt their possibilities or capabilities to perform clinical studies can be turned to professional and efficient medical centers for testing and approving new drugs in a short time – with their own interest taken into account.

• Are you looking for a partner to give you non-binding answers your questions concerning possible participation in clinical studies?
• Do you have doubts concerning the purpose of clinical studies and drug testing or related work procedures?
• Are you not sure whether the equipment of your office or your time and other resources of your team meet the expectations of a clinical study sponsor

We will be happy to explain key processes of clinical studies to you, the responsibilities and involvement of the physician and their team in the study. We will also provide some practical examples.

HOW do we achieve this?

Clinical Research Center s.r.o. builds long-term relationships with selected physicians with various types of expertise in order to test new drugs and treatment options successfully and safely. Our coordinators help physicians and medical centers with preparation, administration, coordination and data entering within the clinical studies. Together, we form a team that can reliably respond to any changes and emergency (mostly capacity-related) situations. We lend any missing technical equipment required for the study execution for the physicians. We explain any complex processes and we search for simple and effective solutions together.

WHAT do we do, WHAT do we offer?

We see to due training of all team members and their substitutability to prevent jeopardizing the progress of testing of new drugs and treatment methods. When providing support to medical centers, our coordinators mostly focus on:

• Study preparation in the center, including introductory trainings of the clinical trial sponsor.
• Patient coordination in accordance with a given study protocol.
• Documentation compilation and data entering in patient data sheets.
• Cooperation and communication with monitors and auditors supervising correct study execution.
• Keeping the investigator site file (ISF) complete.
• Reporting adverse effects and submitting other statutory reports to the ethics committee.
• Processing biological samples for the purpose of pharmacokinetic, pharmacodynamic and pharmacogenetic analysis in cooperation with medical staff.

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.