Drug Approval Process in Europe - An Outlook

Drug Approval Process in Europe - An Outlook Updated Research Available

 

RELEASE DATE
22-Dec-2008
REGION
Europe
Research Code: M2DB-01-00-00-00
SKU: HC01742-EU-MR_06503
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Description

This research deals with the drug approval process in Europe by focussing on the various marketing authorisation procedures, price controls and parallel trading. A snapshot of the biosimilars approval process is also provided along with the key strategic recommendations.

Table of Contents

Executive Summary of the Drug Approval Process in Europe

  • Overview of the European Drug Approval Process

Research Methodology for Drug Approval Process in Europe

  • The Methodology
  • Scope and Objectives

Major Industry Challenges

  • Introduction
  • Regulatory Challenges in the European Union

Marketing Authorisation Procedures

  • Marketing Authorisation Procedures in Europe
  • Comparing the Regulatory Systems in Europe and the United States

Overview of the Price Control and Parallel Trading in Europe

  • Analysis of Price Control and Parallel Trading

Approval Process for Biosimilars

  • Biosimilars in Europe

Key Findings

  • Recommendations for the European Drug Approval Process

Decision Support Database

  • Number of Biotech Companies
  • Number of Biotetchnology Patents-European Patents Office
  • Number of Biotechnology Patents - USA Patents and Trade Mark Office
  • Government R&D Investment in Biotechnology
  • Private Investment in Biotechnology
Related Research
This research deals with the drug approval process in Europe by focussing on the various marketing authorisation procedures, price controls and parallel trading. A snapshot of the biosimilars approval process is also provided along with the key strategic recommendations.
More Information
No Index No
Podcast No
Industries Healthcare
WIP Number M2DB-01-00-00-00
Is Prebook No