A review of generic medicine pricing in Europe

Journal Title: Generics and Biosimilars Initiative Journal - Year 2012, Vol 1, Issue 1

Abstract

Introduction: Switching from originator products to generic equivalents is a key method used by governments to reduce costs and keep their healthcare systems sustainable. The aim of this article is to review generic medicine pricing in Europe by analysing the factors that influence them. Methods: The literature review focused on selected studies that highlighted generic medicine pricing in ambulatory care in Europe. PubMed, the Centre for Reviews and Dissemination databases, Cochrane Database of Systematic Reviews, and EconLit were searched up to August 2011. Search terms included, ‘pharmaceuticals’, ‘generic medicines’, ‘Europe’, ‘pricing’, ‘discount’, and ‘rebate’. Bibliographies of included studies were checked for relevant studies and the status of generic medicines pricing in Europe was also documented via accessing the European Generic medicines Association market survey. Results: Ex-manufacturer prices for generic medicines were found to vary substantially between European countries, which suggests that pricing not only reflects production costs, but is also influenced by the domestic regulatory environment. The penetration of generic medicines is more successful in countries that permit free pricing of medicines than in those that have price regulation. Although tendering systems may reduce (generic) medicine prices in the short term, little is known about the overall long-term impact of such systems. Conclusion: No single approach towards developing generic medicine pricing policies and attaining cost savings was evident.

Authors and Affiliations

Steven Simoens

Keywords

Related Articles

Drug shortages hit US oncologists hard

The number of drug shortages in the US has tripled between 2006 and 2012, with drug shortages now affecting most US oncologists and impacting on patient care. There is a need for new guidelines to control drug substituti...

Tighter EU rules on pharmacovigilance for biologicals

The new EU pharmacovigilance legislation which comes into force in July 2012 will include a tightening of requirements relating to product information and identification, as well as the regulations surrounding biosimilar...

Generics policies–a globally-relevant implementation challenge

Vogler and Zimmerman, reporting on the 2011 Pharmaceutical Pricing and Reimbursement Information (PPRI) Conference, have noted the incomplete application of generics policies in many settings, and have called for more co...

Assessing biosimilarity and interchangeability of biosimilar products under the Biologics Price Competition and Innovation Act

Biological (large molecule) drug products are made via living systems and are complex and variable in nature. As a result, generic forms of biological products, also termed biosimilars in the EU or follow-on biologics by...

Statistical considerations for the development of biosimilar products

As the patents of a growing number of biological medicines have already expired or are due to expire, it has led to an increased interest from both the biopharmaceutical industry and the regulatory agencies in the develo...

Download PDF file
  • EP ID EP355186
  • DOI 10.5639/gabij.2012.0101.004
  • Views 127
  • Downloads 0

How To Cite

Steven Simoens (2012). A review of generic medicine pricing in Europe. Generics and Biosimilars Initiative Journal, 1(1), 8-12. https://europub.co.uk./articles/-A-355186