CRC
CRC - We create medicine
of tomorrow

About us

CRC Co Ltd. is located in Poznan, POLAND, at Poznańska Street 3. This is a private enterprise that conducts clinical trials. We are a modern center participating in commercial research projects in various fields of medicine.

Clinical studies are conducted by specialists with the highest qualifications who have years of experience in clinical trials phase I, II, III and IV. Professional service and the highest quality of performance of medical projects is our priority. We put attention on every detail of our business.

CURRENTLY WE CONDUCT CLINICAL STUDIES IN THE FOLLOWING INDICATIONS:

  • Episodic childhood migraine
  • Chronic childhood migraine
  • Post-polio syndrome
  • Bladder cancer
  • Ulcerative colitis
  • Crohn's disease
  • Study to evaluate the effect of evolocumab on the reduction of cardiovascular events in a patient population at high cardiovascular risk
  • Hot flashes in women during menopause
  • Prostate cancer
  • Primary progressive multiple sclerosis
  • Overactive bladder
  • Myasthenia
  • Depression

IN THE NEAR FUTURE WE PLAN TO START
TRIALS WITH NEW DRUGS FOR:

  • Psoriasis
To submit your candidacy for the study, please complete the form below, and in the "content" please enter a disease from the above list, which you get sick.

For Patient

Clinical studies are commissioned and sponsored by national or international pharmaceutical companies. Their main objective is to evaluate the efficacy and safety of newly discovered drugs, medical devices or methods of treatment Key benefits of the research are:
  • Free access to the latest treatments and new drugs
  • The highest standards of medical care
  • Free laboratory testing and medical diagnostics
  • Constant attendance by the investigator (medical specialist)
Each participant in a research project first goes through a screening. This is the first phase of the study during which the investigator qualifies the subject to the next periods of the study Each patient must meet all entrance criteria to start treatment phase of the trial.

Before entering the study, each patient is fully informed (by Investigator and in written) about study drugs, potential risk, potential benefit, visits schedule, medical procedures, etc. Then patient is requested to sign a form (informed consent for=ICF) acknowledging that he was told of these risks, understands them, and consents to the treatment. Agreement may be withdrawn at any time during the clinical research without giving any reasons and without any consequences for patient.

Your health and safety are a priority for us. All the studies carried out in accordance with the principles of Good Clinical Practice (GCP) regulations.

CONTACT US:

For Doctors

If you are a doctor and you would like to cooperate with us, we offer the chance to expand your job opportunities. Working with us in innovative research projects could be also an additional source of income for you. If you are interested in working with us, we invite you to complete the form below. Please send us a message with the name of specialization, your personal details and phone number. We will contactyou shortly!

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For Sponsors / CRO

We are successfully suporting a qualified staff of specialists in the following medical disciplines: rheumatology, dermatology, neurology, urology, cardiology, gastroenterology, gynecology, oncology, laryngology, psychiatry, hematology, orthopedics.

We have certified equipment necessary to conduct research.

Some of our doctors are very experienced investigators who worked as Principal Investigators and even National Coordinating Investigators a couple of times participating in all phases of clinical trials: I, II, III and IV.

CONTACT US:

Contact

Clinical Research Center Sp. z o.o.
ul. Poznańska 3/31
60-848 Poznań

tel. +48 61 663 24 54
fax. +48 61 663 25 13

biuro@cr-center.pl