Pharma & Medical Device Regulation 2020

Pharma & Medical Device Regulation 2020

Pages: 141

ISBN: 978-1-83862-106-3

  • £300.00

Pharma & Medical Device Regulation provides a timely and comprehensive overview of the latest legislative and regulatory develops affecting this rapidly changing industry. Topics covered include: health services framework and competent authorities; clinical practice; marketing authorisation; amending authorisations; recall’ promotion; enforcement of advertising rules; pricing and reimbursement; off-label use and unlicensed products and sale and supply.  

Published in December 2019, this first edition contains:

Editorial chapters

  • EU antitrust developments in the pharmaceutical sector
    • Axel Schulz, White & Case


  • Australia
  • Austria
  • Colombia
  • Denmark
  • European Union
  • Germany
  • Greece
  • Japan
  • Luxembourg
  • Mexico
  • Serbia
  • Sweden
  • South Korea
  • Switzerland
  • Turkey
  • United Kingdom
  • United States

Alexander Ehlers, Ehlers, Ehlers & Partner Rechtsanwaltsgesellschaft mbB

Alexander Ehlers fully advises health care professionals on all legal and strategic issues, in particular national and international pharmaceutical companies and medical device manufacturers.

The counselling covers all questions of health policy and social law as well as questions concerning the reimbursement of medical services and medicines or medical devices.

In addition, Alexander Ehlers advises companies on regulatory matters.

In addition, his field of activity includes the counseling of medical service providers in the outpatient and inpatient sector (bearer of the German Physicians' Award 2002).

Due to his many years of working in the German health service, Alexander Ehlers has excellent contacts to relevant decision-makers, which are regularly used by clients as part of Public Policy Advisory.

Alexander Ehlers is a frequent speaker at trade congresses and author of numerous publications.

Ian Dodds-Smith, Arnold & Porter Kaye Scholer LLP


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