Resources and links (FMD)

List of resources for background information on the Falsified Medicines Directive and the Delegated Regulation.

Consultation documents:

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)

European Medicines Verification System (EMVS) : 'European Pack Coding Guidelines'

EMVO

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.

EU Commission

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.safetyfeatures@mhra.gov.uk.