Medical Product Consultant certification

Purpose

Participants (according to paragraph 31 of the MPG) of this training will learn both the legal regulatory aspects, as well as the most relevant issues, which arise in a clinic. The result will be that you are clearly informed regarding your level of liability and thus, avoid risks. The training covers a wide range of topics from the general guidelines and regulations to more detailed topics such as Law on Advertising in the Health Care System. The content is simplified and presented in a way that participants can understand. 

Content

  • Profile of a product manager
  • European and German legal guidelines
  • Medical Devices Act Germany
  • Medical device manufacturer compliance
  • Product classification and description
  • Market monitoring and Medical device vigilance system
  • Law on Advertising in the Health Care System
  • Amendments to the medical device laws and regulations 

 

Lecturer

Specialists with many years of experience in healthcare economy

New Dates in 2017

17th of March2017

28th of April 2017

26th of May 2017

23rd of June 2017

Cost

380,00 € (excludes VAT)

Course fees include all learning materials, certification, and refreshments.

Upon completing the course each participant will receive a certificate. Please see our brochure for more information regarding registration.