FAQs

The Falsified Medicines Directive lays down the rules for the manufacture, import, marketing and supply of medicinal products. It also makes sure the internal market for medicinal products works as it should while ensuring the protection of public health in the EU.

For additional help and information on this registration process and requirements please visit our 'Falsified Medicines Directive: Registration of manufacturers, importers and distributors of active substances' page on the http://www.mhra.gov.uk site