Application support from A to Z

NUB-, OPS-, ICD-, DRG-, EBM- and Medical Devices Catalogue Applications, etc…

The conditions of the regulatory institutions are the next authority beneath the national and international laws. The legislator has assigned these tasks to the appropriate institutions. As a result of this, the specific regulatory requirements and processes vary between the ambulatory and the stationary sector. Nevertheless, there are sufficient possibilities to successfully configure the applications.

An overview of the most important applications:

  • Application for the listing of medical devices in the official catalogue § 139 SGB V
  • Application for an institutional sign and number
  • Application for the CE mark
  • Application for the inclusion on the list of prescribable medicinal products (Anlage V der Arzneimittelrichtlinie)
  • Application for counselling at theG-BA (§§ 135 & § 137 SGB V)
  • DRG-Application
  • EBM-Application
  • ICD-Application
  • NUB-Application
  • OPS-Application
  • PZN-Application

 

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