➡ Experienced team, backed by 18 years of experience in clinical trial monitoring.
➡ In-depth knowledge of GCP principles, ALCOA++ and familiarity with IT tools used during the project.
➡ Guarantee of data of the highest quality.
➡ Timely implementation.
➡ Implementation with respect for the highest ethical standards.
➡ Our long-standing presence in the industry, is guaranteed to provide comprehensive support for clinical
trials in a broad spectrum of therapeutic areas such as:
Diabetology
Cardiology
Gastroenterology
Neurology
Rheumatology
Rare diseases
Dermatology
Vaccines
Alergology
Pulmunology
Urology
Nephrology
Ophthalmology
Throughout our career, we have prioritized not only the quality of the data but, above all, the patients
well-being participating in clinical trials. We have always acted according to the highest ethical standards
and professionalism.
Our passion, knowledge and skills in crisis management have resulted in positive results from numerous
audits by both Study Sponsors and by such demanding institutions as the FDA.
While creating our center, we aimed to create a place where every patient is treated with the utmost
respect and care.
We believe that clinical trials are an opportunity to access innovative therapies that can improve patients
quality of life. Our mission is to provide patients with the opportunity to participate in trials that can
contribute to the development of new drugs and therapies, thereby improving the health of future
generations.
Clinical Study Center S.C.
ul. Kamieńskiego 215/U3
51-124 Wrocław
NIP 8952283110 REGON 540762973-00012
RPWDL 000000287651