The below is a list of resources for background information on the Falsified Medicines Directive and the Delegated Regulation.
Memorandum of Understanding (MoU) 'On the Formation and Governance Model of a Joint Stakeholder-Run Verification System of Pharmaceutical Products in the UK' (June 2016)
European Medicines Verification Organisation: Requirements for the European Medicines Verification System – URS Lite (May 2016)
The European Medicines Verification Organisation (EMVO) is pleased to announce that the EMVO On-boarding Partner Portal (OBP Portal) is up and running. To facilitate the on-boarding of pharmaceutical companies to the EU Hub, the user-friendly web-based portal will guide pharmaceutical companies step by step through the process.
The MHRA publish a regular newsletter with helpful information for stakeholders, including updates on the latest developments and progress with implementing the FMD Delegated Regulation. This can be accessed via MyABPI through this link.
For more information, and to register for their distribution list, please contact Ciara Dunne.
Recent article from the Pharmaceutical Journal 'Brexit won't stop UK implementation of Falsified Medicines Directive '