We understand the requirements of the Falsified Medicines Directive (FMD)
By February 2019, pharmaceutical packaging including prescription drugs and high risk over-the-counter medicines must comply with The Falsified Medicines Directive (2011/62/EU). (FMD)
This directive places 2 demands on the product packaging:
All packs should carry a unique serial number to identify and authenticate individual products.
Packs should be sealed in a way that visibly enables tamper verification.
Whether you are a pharmaceutical manufacturer, pharmacy contractor, distributor or retailer, email or call us now to find out more about how we can help you comply with The EU Falsified Medicines Directive (FMD).
For more information on The Falsified Medicines Directive (2011/62/EU) click here
To contact us, please send an email to firstname.lastname@example.org or call us on +44 (0)1543 431070