The evolving process of European combination product review, Part I.

نویسنده

  • Maria E Donawa
چکیده

A new European guideline on drug-eluting stents (DES) introduces for the first time detailed information that European drug authorities should review concerning the medicinal substance that is incorporated into this type of drug-device combination product. Part I of this article discusses European requirements that apply to DES. Part II will discuss the new guideline, other stent guidelines and evolving process of drug-device regulatory review in Europe.

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The evolving process of European combination product review, Part II.

A new European guideline on drug-eluting stents (DES) introduces for the first time detailed information that European drug authorities should review concerning the medicinal substance that is incorporated into this type of drug-device combination product. Part I of this article discussed European requirements that apply to DES. This article discusses the new guideline, other stent guidelines, ...

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عنوان ژورنال:
  • Medical device technology

دوره 19 6  شماره 

صفحات  -

تاریخ انتشار 2008