rpp reseach and partnership platform contribution by dr
play

RPP Reseach and Partnership Platform Contribution By Dr Sven - PDF document

Intergovernmental Group of Experts on Competition Law and Policy, Fifteenth Session Geneva, 19-21 October 2016 RPP Reseach and Partnership Platform Contribution By Dr Sven Gallasch Centre for Competition Policy, United Kingdom Dr Mor Bakhoum -


  1. Intergovernmental Group of Experts on Competition Law and Policy, Fifteenth Session Geneva, 19-21 October 2016 RPP Reseach and Partnership Platform Contribution By Dr Sven Gallasch Centre for Competition Policy, United Kingdom Dr Mor Bakhoum - Max Planck Institute for Innovation and Competition, Germany The views expressed are those of the author(s) and do not necessarily reflect the views of UNCTAD

  2. Increasing the access to affordable medicine in developing countries and LDCs: between regulation and competition Dr Sven Gallasch Dr Mor Bakhoum Centre for Competition Policy, Max Planck Institute for Innovation United Kingdom and Competition, Germany competitionpolicy.ac.uk

  3. Background Developed world • Complex interplay of IP/Competition/pharma regulations • Brand/generic dichotomy • Prone to regulatory gaming – pharma antitrust Developing world • same dichotomy not necessarily applicable • Less prevalent interplay – to a certain extent unknown • How to increase access to affordable medicines through regulation and competition while avoiding regulatory gaming

  4. Project – main research objectives 1. The status quo: identifying the relevant framework 2. Identifying barrier for entry to the pharmaceutical market 3. Providing advice on the improvement of access to affordable medicine

  5. Project – the approach 1. Data collection Creation of panel data set through questionnaires, surveys and structured interviews 2. Empirical research Qualitative data analysis on a country by country basis and later on comparative basis 3. Policy recommendations min: comprehensive overview of access max: compare and delineate individual approaches

  6. Project – categories of variables • Pharmaceutical regulations • Incl. marketing authorisation, drug price regulation, substitution laws, parallel trade • Competition legislation • Incl. US/EU model, policy goals, covering regulated markets, IP exemption, enforcement level, compulsory licensing • IP legislation • Incl. TRIPS, patent enforcement system (bifurcation)

  7. Project – categories of variables (cont) • Procurement • Sector specific information • Incl. supply side, demand side (buyer power, distribution, public/private health) • Anticompetitive conduct

  8. Questions and suggestions? Please contact us: Sven Gallasch s.gallasch@uea.ac.uk Mor Bakhoum mor.bakhoum@ip.mpg.de

Download Presentation
Download Policy: The content available on the website is offered to you 'AS IS' for your personal information and use only. It cannot be commercialized, licensed, or distributed on other websites without prior consent from the author. To download a presentation, simply click this link. If you encounter any difficulties during the download process, it's possible that the publisher has removed the file from their server.

Recommend


More recommend