Changes to IMB processes for variation applications for human and veterinary medicines from 1 August 2010 - updated December 2010
17 February 2011
This guide is intended to provide updated information to stakeholders on changes in the way that the Irish Medicines Board (IMB) processes variation applications for both human and veterinary medicines following the introduction of the new ‘Variations Regulation’ in Ireland.
Changes to IMB processes for variation applications for human and veterinary medicines from 1 August 2010 - updated December 2010