FMD: The Falsified Medicines Directive: Useful Resources

The Falsified Medicines Directive deadline of the 9th February 2019 is fast approaching.

As stakeholders from all areas of the pharmaceuticals market in the EU continue their preparation for this legislation here are several resources that may be useful going forward.

FMD Resources

• European Commission: Falsified Medicines Directive Details
  • Link: https://ec.europa.eu/health/human-use/falsified_medicines_en

• European Commission: Falsified Medicines Directive: Safety Features Delegated Act: Q&A
  • Link: https://ec.europa.eu/health/sites/health/files/files/falsified_medicines/qa_safetyfeature_en.pdf

• HPRA: Health Products Regulatory Authority: Ireland: Falsified Medicines Legislation Details
  • Link: http://www.hpra.ie/homepage/medicines/special-topics/falsified-medicines-legislation

• The Pharmaceutical Journal: Infographic: FMD How it will work
  • Link: https://www.pharmaceutical-journal.com/news-and-analysis/infographics/falsified-medicines-directive-fmd-how-it-will-work/20204433.article

• GS1 UK: The Falsified Medicines Directive
  • Link: https://www.gs1uk.org/our-industries/healthcare/recent-legislation/the-falsified-medicines-directive

• EMVO: The European Medicines Verification Organization
  • Link: https://emvo-medicines.eu/

• IMVO: The Irish Medicines Verification Organization
  • Link: http://www.imvo.ie/

• SecurMed: UK Medicines Verification Organization
  • Link: https://www.securmed.org.uk/

If you need help regarding the FMD and what is required from a compliance perspective, call us on +353 (0)1 827 0650 or email us at info@bds.ie.

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