[Approval of new medicinal products - documentation requirements]

Ugeskr Laeger. 2019 May 20;181(21):V10180678.
[Article in Danish]

Abstract

In this review, we discuss the approval of new medicinal products, which particularly for new products containing a new active substance is increasingly done in collaboration between the European countries. This collaboration has strengthened and harmonised the scientific basis for approval of new drugs in the EU.

Publication types

  • Review

MeSH terms

  • Documentation*
  • Drug Approval*
  • Europe
  • European Union
  • Legislation, Drug*