GMP: New MHRA Q & A Document on the Import of Active Pharmaceutical Ingredients
In article 46 b of Directive 2011/62/EU it lays down strict rules for the import of active ingredients in the EU. Each import from countries outside of the EU must be accompanied by a written confirmation. The answers given in the Q & A document show how the United Kingdom deals with the new situation.
Źródło wiadomośći: http://www.gmp-compliance.org/eca_news_3464_7675,6339,7817.html