ЕЛА (EMA) опубликовало проект руководящего принципа по производстве готовой лекарственной формы (Part I)
- 26 августа 2015
On 9 July 2015, EMA released for 6 months public consultation the Draft guideline on manufacture of the finished dosage form. It should be mentioned here, that the need to update and revise the CPMP/QWP/486/95 note for guidance on manufacture of the finished dosage form (current guideline) was originally presented in the document entitled Concept