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)

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.

EU Commission

MHRA Portal and Guidance

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.

Pharmacy

SecurMed UK

Further information

Recent article from the Pharmaceutical Journal 'Brexit won't stop UK implementation of Falsified Medicines Directive'