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 System (EMVS) : 'European Pack Coding Guidelines'
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.
- Here is the link to get access to the EMVO OBP Portal.
- Website and accompanying resources on FMD, including on-boarding guidance for manufacturers.
MHRA Portal and Guidance
- Implementing the Falsified Medicines Directive: Safety Features
How to prepare for implementation and compliance of the Safety Features Regulation.
The MHRA publish a regular newsletter. To join the mailing list provide your name, your organisation (if applicable) and your title (if applicable) to FMD.firstname.lastname@example.org.
Recent article from the Pharmaceutical Journal 'Brexit won't stop UK implementation of Falsified Medicines Directive'