Ȩ Ä«Å×°í¸® ¸ÂÃãÇü½ÃÀåÁ¶»ç ±¹Á¦ÄÁÆÛ·±½º ±Û·Î¹ú ÆÄÆ®³Ê ¸ÞÀϸµ ¼­ºñ½º ȸ»ç¼Ò°³È¸»ç¼Ò°³ Contact Us
English Japaness Chinese
Home > ½ÃÀ庸°í¼­ > ÆÄ¸Ó½´Æ¼Äà > Á¦³×¸¯ ÀǾàǰ > Pricing and Reimbursement Issues for Generics & Biosimilars Markets in Europe
Ä«Å×°í¸®
ÆÄ¸Ó½´Æ¼Äà (4931)
°¨¿°Áúȯ (349)
°ñÁúȯ Ä¡·á (38)
´ç´¢º´ (194)
¹é½Å (181)
ºñ¸¸Ä¡·á/´ÙÀÌ¾îÆ® (44)
ºñó¹æ ÀǾàǰ (152)
¼öÀÇÇÐ (17)
½Å°æÁúȯ (174)
½Å¾à°³¹ß (1529)
¾ÏÄ¡·á (941)
¾à¹°Àü´Þ (185)
ÀǾàǰ ±ÔÁ¦È¯°æ (127)
Á¤½ÅÁúȯ (86)
Á¦³×¸¯ ÀǾàǰ (128)
Á¦¾àȸ»çºÐ¼® (523)
󹿾à (165)
½ÃÀ庸°í¼­

Pricing and Reimbursement Issues for Generics & Biosimilars Markets in Europe

¸®¼­Ä¡»ç Frost & Sullivan
¹ßÇàÀÏ 2006³â 12¿ù »óǰÄÚµå 48391
ÆäÀÌÁö Á¤º¸ 51 Pages
°¡°Ý
US $ 6,500 £Ü 7,744,700 Web Access (Regional License)
US $ 7,000 £Ü 8,340,500 Hard Copy & Web Access (Regional License)


¿µ¹®¸ñÂ÷

Abstract

This Frost & Sullivan research service titled Pricing and Reimbursement Issues for Generics & Biosimilars Markets in Europe provides a detailed analysis of various issues affecting pricing and reimbursement decisions of generics in Europe. The study includes an overview of cost-containment measures such as reference pricing, parallel trade, generic substitution, patient co-payments and reimbursement. Certain key issues such as the EU accession, the Roche/Bolar provision, data exclusivity and marketing authorisation applications are also discussed.

Table of Contents

1. Executive Summary

  • 1. Executive Summary
    • 1. Executive Summary

2. Glossary of Terms

  • 1. Important Terms
    • 1. Definitions

3. Research Methodology

  • 1. Methodology Of Research
    • 1. The "12 Step" Market Engineering Research Methodology and Process

4. Introduction

  • 1. Overview
    • 1. Market Analysis
    • 2. Scope and Objectives
    • 3. Pricing and Reimbursement
    • 4. The Biosimilars Opportunity

5. Key Trends

  • 1. Pharmaceutical Cost-containment Measures
    • 1. Reference Pricing
    • 2. Parallel Trade
    • 3. Generic Substitution
    • 4. Patient Co-payments and Reimbursement
  • 2. Political/Legal/Regulatory Issues
    • 1. Impact of EU Accession
    • 2. The Roche/Bolar Provision
    • 3. Data Exclusivity and Marketing Authorisation Applications

6. Country-wise Policy Analysis

  • 1. Group I
    • 1. Denmark
    • 2. Germany
    • 3. The Netherlands
    • 4. The United Kingdom
  • 2. Group II
    • 1. Austria
    • 2. Belgium
    • 3. France
    • 4. Italy
    • 5. Portugal
    • 6. Spain
  • 3. Group III
    • 1. Central and Eastern Europe (CEE)

7. Market Participants

  • 1. Market Players
    • 1. List of Generics Market Participants
    • 2. List of Biosimilars Market Participants

8. Strategic Recommendations

  • 1. Recommendations to Market Participants
    • 1. Strategic Suggestions

9. Decision Support Databases

  • 1. DSDs
    • 1. Total Healthcare Expenditure
    • 2. Pharma R&D Expenditure

List of Figures

Chapter 4

  • Generics Market: Market Share of Generics by Value and Volume (Europe), 2004

Chapter 5

  • Generics Market: Country-wise Policy on Generic Substitution (Europe), 2006
  • Generics Market: Average Time Required for Pricing and Reimbursement Approvals (Europe), 2004

Chapter 7

  • Generics Market: List of Key Market Participants (Europe), 2006
  • Biosimilars Market: List of Key Market Participants (Europe), 2006
Back to Top