Update to the legal framework of medicinal products in Portugal

 

The Decree-Law no. 26/2018 which changes the legal framework of medicinal products for human use, implementing the Directive (EU) 2017/1572 laying down the principles and guidelines of good manufacturing practice, was published today in Portugal. Additionally, this Decree-Law transposes the measures set out in Directive 2011/62/EU regarding safety features that shall appear on the packaging of medicinal products for human use and that allow their identification and authentication.

The Decree-Law comes into force on May 2, 2018.

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