PvNET Blog

Global regulations are harmonizing and moving towards ICH and ISO standards with the need of consistently identifying medicinal products across geographies. This in recent times has come up as an EMA regulatory requirement for xEVMPD, with the objective of clear identification of medicines in reports. PvNET’s xEVMPD solution meticulously addresses this regulatory requirement, generating xEVPRMs per schema laid down in accordance with Article 57 (2) requirements.