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tasks at clinical
trial sites
monitor and rethink
our processes
for sustainability
equality
is essential
for us
importance of the
quality of training,
which is the key to
the quality of work
provide patients with
up to date treatments
that will only become
universally available
in years to come
on how we protect
the environment,
so we support every
solution for green office
About us
Since 2007, Clinical Research Coordination Ltd. has been providing assistance to customers and investigational sites in conducting human clinical trials.
Our system effectively integrates clinical research into daily patient care.
The result of our continuous development is a 50-100% improvement in the qualitative and quantitative performance of our partner sites.
We are currently coordinating more than
500 clinical trials in 16 institutions.
Katalin Boér, MD, PhD
“With our daily clinical routine, it would be impracticable for us to conduct clinical trials without the help of coordinators. Based on my many years of experience, I can confirm that involving coordination into the clinical trials was a right choice. CRC works with well-trained colleagues and we always get coordinators who can fit in well with our team. Without coordinators, it would be inconceivable to conduct clinical trials in our department.”
habil. Miklós Garami, MD, PhD
“CRC provides personalized help both for me and my staff. They take over from our principal investigators and subinvestigators the communication with sponsoring partners, the organization of clinical trials and the related administrational tasks, thus facilitating the involved physicians’s work in our clinic. This allows us to enroll more patients than ever before with less overwork.”
Péter Hauser, MD, PhD
“I am not worried if I know that CRC is carrying my clinical trials.
Accurate, precise, proactive, reliable… I just have to look at the patient.”
med.habil. István Láng, MD, PhD, DSc
Oncologist, Doctor of Internal Medicine, Allergologist, Clinical Immunologist and Clinical Pharmacologist
Professor of Semmelweis University, Retired Head of Dept.of the National Institute of Oncology, Head of Dept.of Oncology at the Istenhegyi Gene Diagnostic Center
Dániel Berczki, MD, PhD, DSc, FESO
Professor of Neurology, Semmelweis University
“CRC has been assisting the Department of Neurology for two years under the leadership of Attila Kiss.
One of the limitations of patient involvement in the international multicentre studies is the lack of ti-me, that is why we appreciate the administrative help of the CRC staff in addition to „multitasking” (treatment, education, research). It is a pleasure to work with their polite and precise colleagues.”
György Losonczy, MD, PhD, DSc
Retired Head of Department of Pulmonology, Semmelweis University
“Assistance of CRC greatly facilitates to conduct clinical trials. Their work is reliable, accurate and fast. They provide essential help to arrange the multilateral contracs, and obtain new clinical trials for the study site. They have a polite staff.”
Laszló Landherr, MD, PhD
Head of Department of Oncoradiology, Uzsoki Hospital
“Clinical trials have also undergone an evolution. Nowadays, it is inconceivable for a clinician to do this type of research without professional help. I’ve known and worked together with the CRC team for a decade and I can only say the best about them. Both their competence and their ability to cooperate are first class. We have participated in 65 clinical trials in the last 5 years with their help, and it would have been unthinkable without them.”
Tibor Martyin, MD
“Many years ago, the sponsor provided a qualified, experienced coordinator to conduct a clinical study (she was a colleague of CRC). That was when I really saw what is the difference when working with a coordinator, and since then, I have been relying on CRC for each clinical study. I really like that their colleagues always strive for the high quality, professional work, which appears to the other participants in the study (clinical study staff, patients, CRA, sponsor). This way we have been able to increase both the number of the clinical studies and the number of the patient’s enrollments.”
Gábor Csáki, MD
“We got in touch with CRC Kft. in connection with an AO study wich demanded a lot of administrative work. CRC staff have shouldered the burden of mailing and completing CRFs so we can concentrate on the surgical care of patients. Thank You.”
med.habil. Erika Hitre, MD, PhD
“Clinical trials are essential for up-to-date oncology care, as patients can be provided with state-of-the-art treatment. And clinical trials are difficult to imagine without highly qualified coordination. That is what I found in CRC. We have been working together since the foundation of the company, which has been efficient and smooth ever since.”