• Falsified Medicines legislation and the process of API import from Third Countries (published 1 July 2013) | pdf

• Falsified Medicines Directive - HMA concerns regarding the adoption of the new Directive (published on 10 December 2012) | pdf

Directive 2011/62/EU article 85b.2 establishes that a register of persons brokering medicinal products shall be publicly accessible. The HMA Falsified Medicines Directive Task Force has coordinated a list of registered brokers which will facilitate the verification by wholesalers as established in article 80(d).