Clinical trials has been conducting in hospital since 1995r.
Our aim is to conduct clinical trials according to the Good Clinical Practice (GCP) guidelines developed by the International Conference on Harmonisation (ICH) and the principles contained in the World Medical Association Declaration of Helsinki on the ‘Ethical Principles for Medical Research Involving Human Subjects’ .
Our team is made up of specialists with experience in clinical trials. We know that medical research requires not only high medical qualifications but also highly specialized knowledge about clinical trials conduction. Centre has developed special training program available for Investigators and Clinical Research Coordinators. They cover issues such as gaining informed consent from trial participants, safety reporting and quality assurance.
The welfare and safety of our patients comes first.
Our clinical studies
It is possible to conduct PHASE I - IV Clinical Trials concerned with Medical Devices and Drug Development in Cardiology, Anesthesiology and Intensive Care, Surgery and Angiosurgery, Laryngology, Neurology, Oncology and Chemotherapy, Nephrology, Dermatology, Urology, Pediatrics, Neonatology, Gynecology and Obstetric, Ophthalmology, Psychiatry, Rheumatology).
Our Center have been successful in recruiting large numbers of patients to clinical trials. Strategies for recruitment and compliance are the subject of our ongoing evaluation.
Our internal effective management of clinical programs allows us to organize clinical study on high international standard (enhance of research protocols and Sponsors/CRO standard operating procedures, quick query resolution, very good facilitates and equipment, proper study material storage, study close out and archiving).
Our IT infrastructure
Hospital has new IT infrastructure with broadband internet access and IT service available between 7a. and 7 p.m every day.
Our Ethics Committee
Ethics Committee Affiliated in Research and Development Centre of our hospital is able to provide opinion on clinical research projects.
Quality results in a timely manner
- Ischemic heart disease (acute coronary syndromes: unstable angina, myocardial infarction non-ST segment elevation myocardial infarction (NSTEMI) and ST segment elevation myocardial infarction (STEMI)
- Heart failure
- Systemic hypertension
- Thromboembolic Diseases (pulmonary embolism)
- Atrial Fibrillation
- Breast Cancer
- Kidney Cancer
- Malignant neoplasm of the large intestine
- Lung cancer
- Benign/malicious prostate tumour
Surgery and Angiosurgery
- Deep venous thrombosis
- Leg ulcers associated with chronic venous insufficiency
- Acute and chronic lower limb ischemia
- Skin and soft tissue infections
- Renal insufficiency in diabetic patients
- Kidney transplantation
- Treatment of anemia in hemodialyzed and not hemodialyzed patients with renal insufficiency
- Seborrheic dermatitis
- Acute bacterial sinusitis
- Chronic sinusitis
- Peptic ulcer
- Diabetes mellitus
We would like to ease the administrative burden associated with conducting clinical research, including clinical trials agreements preparation. We would like to offer preparation of agreement template which could be used during long cooperation with CRO/Sponsor.
“From contract signature to study closure” dedicated team is responsible for overseeing each study and delivering the data on time.
Małgorzata Mikulewicz M.D, PhD.
Hospital’s Management Representative on Clinical Trials Research and Development Centre