- ISO Identification of Medicinal Products (IDMP)
- Extended Eudravigilance Medicinal Product Dictionary (XEVMPD)
- Electronic Regulatory Affairs
- Regulatory Operations
More detail of the services that can be provided can be seen here.
Andrew Marr had 27 years of leading-edge experience working within Regulatory Affairs/Regulatory Operations of a major pharmaceutical company plus leading roles in numerous industry/regulator collaborative projects, including as chairperson of ICH Expert Working Groups and of the PIM programme. He has been the leading consultant on XEVMPD and the ISO IDMP standards since setting up Marr Consultancy Ltd in 2011.
Andrew is a recognised thought-leader on the creation, management and exchange of
electronic information between industry and regulators. (read more)