Breadcrumb
Breadcrumb
Faculty of Medicine
Tartu linn, Tartumaa
EST
Centre for Doctoral Studies in Medicine and Sport
Department of Biochemistry
Chair of Medical Biochemistry
Department of Pharmacology
Chair of Pharmacology and Toxicology
Chair of Clinical Pharmacology
Department of Physiology
Chair of Physiology
Department of Biomedicine
Molecular Pathology Research Group
Laboratory of Precision and Nanomedicine
RNA Biology Research Group
Chair of Human Genetics
Chair of Human Biology
Laboratory Animal Centre
Department of Immunology
Department of Pathophysiology
Department of Anatomy
Chair of Human Anatomy
Chair of Histology and Embryology
Chair of Surgical Anatomy
Department of Microbiology
Chair of Medical Microbiology and Virology
Research Group of Human Microbial Ecology
Research Group of Clinical Microbiology
Research Group of HIV Studies
Department of Pathological Anatomy and Forensic Medicine
Chair of Pathological Anatomy
Chair of Forensic Medicine
Department of Anesthesiology and Intensive Care
Department of Hematology and Oncology
Department of Surgery
Department of Pulmonology
Department of Oto-Rhino-Laryngology
Department of Pediatrics
Department of Dermatology and Venerology

Department of Obstetrics and Gynecology
Department of Neurology and Neurosurgery
Department of Psychiatry
Department of Radiology
Department of Ophthalmology
Department of Internal Medicine
Department of Sports Medicine and Rehabilitation
Department of Cardiology
Department of Traumatology and Orthopedics
Centre of Continuing Education
Department of Clinical Genetics
Clinical Research Centre

CV in Research Information System
Competence: Advising on general research questions; counselling a procedure for conducting clinical research at Tartu University Hospital Clinics and a selection of research centres; advising on the budgeting of a planned project. First contact on any issue related to clinical trial planning. Certified expert in Good Clinical Practice.

CV in Research Information System
Competence: Counselling issues related to biobanking – storage of samples, databases etc.

Competence: 18 years of experience in the international clinical research field with various indications in phase I to IV clinical trials. Monitoring of clinical trials from pre-study visit to study closure visit. Advising and compiling applications for Ethics Committee and State Agency of Medicines. Advising and compiling standard operating procedures (SOP) used in clinical trials.

CV in Research Information System
Competence: Counselling issues related to biobanking – storage of samples, databases etc.