Changes to IMB processes for variation applications for human and veterinary medicines from 1st August 2010 - updated December 2010
09 July 2010
This guide is intended to provide 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 took effect from 1st August 2010.
Click on the link below to read the guide outlining the changes:
Changes to IMB processes for variation applications for human and veterinary medicines from 1st August 2010 - updated December 2010