Welcome to eRegulatory-Affairs.com
eRegulatory-Affairs Consulting provides analyis, consulting, solutions for Pharma Companies looking for advice and guidance
in the complex regulated enviroment.
This includes topics form registration planning and tracking and dossier and submission content planning up to XEVMPD
reporting to the European Medicines Agency (EMA) but also solutions for label management.
eRegulatory Affairs uses experience gained with customer projects as well as experience used when working with the
Authorities on the development of upcoming standards.