Research factors that are critical (or critically important) in assessing effectiveness of the pharmacovigilance platform.

Factors that determine the effectiveness of the digital pharmacovigilance database are considered in the example of the development and
analysis of the OtiPharm® Data Pro platform. Factors were divided into two groups: highly specialized, in which compliance with legal
requirements for pharmacovigilance has the highest-priority; and non-specialized, that influence on the user experience of experts when
working with the system. Such stages of pharmacovigilance processes as medicine safety data collection, processing and structuring and
reporting to regulatory authorities are subject to automation.