GOOD CHOICE FOR
SPONSORS / CRO
We have been cooperating with CRO for 20 years as trustworthy partners. We are characterized by speed, efficiency and high quality of operation.
What are your gains?
20 years of experience and dozens of conducted clinical trials from I to IV phase make us trustworthy partners. We guarantee projects completion on time and in line with the highest standards.
Fast feasibility process
Specialized organizational structure
Efficient recruitment
of patients
Quality control
at every stage
Benefits for sponsors/CRO

  • A partner with well-established experience based on hundreds of clinical trials in various fields of medicine.
  • Fast start and clinical trials completed on time.
  • Modern sites in convenient locations in Poland.
  • A team of highly qualified investigators and administrative staff.
  • Specialized organizational structure in each of the sites.
  • Efficient recruitment of patients using our proprietary methods.
  • Modern medical equipment and strict operational procedures
  • Accurate quality monitoring at every stage of the project.
  • Clinical trials conducted in line with global trends.

 

20 years of experience.

Our experience is based on nearly 20 years of practice. We have conducted several hundreds clinical trials from the first to the fourth phase in many branches of medicine. Each clinical trial is managed by highly qualified investigators.

 A specialized organizational structure.

Currently, over 100 investigators are employed in our centers. The area of management, administration and medical support is a specialized organizational structure, which includes experienced coordinators, medical assistants, data controllers, and nurses and lab technicians.

Fast start and effective recruitment.

We guarantee a fast feasibility process and a short preparation period before launching the project (about 4 weeks on our part). This stage is entrusted to a specialized START-UP team. Patient recruitment is assisted by a dynamic team supporting doctors and conducting information campaigns among patients using traditional and modern tools. Extensive bases of potentially interested people, online campaigns or efficient call centers enable us to  conduct recruitment activities effectively.

Quality control

Thanks to the location in well-functioning hospitals (or in their vicinity), our sites have access to high quality diagnostic and laboratory equipment. We have 24/7 monitored and dedicated archives for medical records, protection against unauthorized access, and procedures and systems to protect against the loss of collected data. One of our advantages, ensuring the quality, timeliness and effectiveness of conducted clinical trials, is the management system based on standard operating procedures (SOP) and supported by innovative IT tools.

Our doctors have extensive experience in conducting clinical trials primarily in the field of:
  • CARDIOLOGY – coronary heart disease, myocardial infarction, hypertension, arrhythmias, heart failure; ENDOCRINOLOGY AND DIABETOLOGY- type 2 and type 1 diabetes, complications in diabetes – diabetic foot, diabetic polyneuropathy;
  • METABOLIC ILLNESSES- obesity, lipid disorders;
  • NEUROLOGY – stroke, polyneuropathy, Alzheimer’s disease, multiple sclerosis, analgesic treatment;
  • RHEUMATOLOGY – RA, degenerative disease, gout;
  • PULMONOLOGY – bronchial asthma, COPD;
  • GASTROLOGY – Crohn’s disease, ulcerative colitis, irritable bowel;
  • INFECTIOUS DISEASES- viral hepatitis
  • DERMATOLOGY – psoriasis, atopic dermatitis, acne;
  • OBSTETRICS AND GYNECOLOGY – candidiasis of vulva and vagina;
  • NEPHROLOGY – renal failure, albuminuria, diabetic nephropathy;
  • ONCOLOGY – lung, pancreas, stomach, prostate, bladder, reproductive organs, kidney, liver, bronchus and lung, cervix and prostate cancer;
  • HEMATOLOGY – leukemia, myelomas;
  • CLINICAL IMMUNOLOGY
  • UROLOGY
  • AND OTHERS

We will respond to every clinical trial proposal, and we will implement the feasibility process with due diligence in the shortest possible time. Our START-UP Team is at your disposal. After the initial acceptance of the clinical trial, contracting and business negotiations are finalized (from our side) most often to 4 weeks.

 

Contact our START-UP team:

TEL.: 81 506 50 20

KOM.: 533 691 047

E-MAIL: feasibility@komed-ck.pl