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Is medicines parallel trade 'regulatory arbitrage'?

Joan Costa-Font1

  • 1Department of Social Policy, London School of Economics and Political Science (LSE), Houghton Street, London, WC2A 2AE, UK. j.costa-font@lse.ac.uk.

International Journal of Health Economics and Management
|November 24, 2016
PubMed
Summary

Parallel trade in medicines is driven by regulatory differences, not just price. This study shows that varying distribution margins significantly influence parallel import flows, suggesting a form of regulatory arbitrage.

Keywords:
Parallel importsParallel tradePharmaceuticalsRegulatory arbitrageSupply chain

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Area of Science:

  • Health Economics
  • Pharmaceutical Distribution
  • Regulatory Policy

Background:

  • Parallel trade (PT) involves diverting patented medicines through alternative distribution channels.
  • While often viewed as common arbitrage, PT may represent regulatory arbitrage with unequal welfare effects.

Purpose of the Study:

  • To investigate whether cross-country differences in statutory distribution margins, beyond price, drive parallel medicine imports.
  • To test the hypothesis that parallel trade in pharmaceuticals constitutes regulatory arbitrage.

Main Methods:

  • Utilized a unique dataset of parallel imported medicine sales (statins) to the Netherlands.
  • Employed a gravity model and instrumental variable strategy to analyze price and distribution margin impacts.
  • Focused on a therapeutic group accounting for 5% of the market with no generic competition.

Main Results:

  • Parallel imports were significantly driven by cross-country differences in statutory distribution margins.
  • Price differences also contributed to parallel import flows.
  • Findings support the hypothesis that PT is a form of regulatory arbitrage.

Conclusions:

  • Statutory distribution margins are a key determinant of parallel medicine trade flows.
  • Parallel trade in pharmaceuticals functions as regulatory arbitrage, influenced by differing national regulations.
  • Policy implications include considering the impact of distribution regulations on medicine markets.