We can ensure monitoring and evaluation of drug safety, collection and analysis of information on adverse events to minimise risks, ensure patient safety, support regulatory processes - comprehensive and partial services in the field of local pharmacovigilance:

• Safety monitoring during research projects
• Setting up processes to identify, collect, report, monitor and analyze adverse events, including serious and unexpected ones
• Preparation of Line-listing, Annual Safety Report for clinical trials of medicinal products
• Adverse event reporting through the Eudravigilance database