The aim of the Laboratory is to ensure that the clinical trials are performed according to the experimental protocol, the GoodClinical Practice (GCP), and the rules required.
The task of Laboratory researchers is to arrange and planning the clinical trials following a correct methodology, ensure the monitoring of the data collected, ensure the timely recording and reporting of adverse events (pharmacovigilance) and coordinate the management of the experimental product during all stages of the research.
Clinical Investigation of phases I, II and III
Pharmacovigilance and clinical and pharmacological investigations
International Consensus on Cardiopulmonary Resuscitation.