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EU における医薬品・バイオテクノロジー業界のビジネスチャンスに関する戦略的分析

Strategic Analysis of the Opportunities for the Pharmaceutical and Biotechnology Industry in the 'New' EU Countries

発行 Frost & Sullivan
出版日 2004年12月 商品コード 26336
ページ情報 英文  
価格
こちらの商品の販売は終了いたしました。

当商品の販売は、2011年07月19日を持ちまして終了しました。

原文目次

Abstract

The addition of new countries to the European Union (EU) has changed the dynamics within its healthcare industry, which is now the second largest industry in the world following North America. As these new members work towards raising standards to meet EU guidelines, investments are also on the rise. The new member countries are focusing on creating long-term sustainable systematic changes internally to increase productivity and profitability. Following these initiatives and regulations, the market is expected to grow at a consistent rate.

This Frost & Sullivan strategic analysis looks at the opportunities in the pharmaceuticals and biotechnology industry in the new EU countries. It offers an overview on healthcare sectors and accurate facts on the burgeoning EU markets. The research includes challenges related to the industry and revenue opportunities along with vital information on clinical trials and strategic positioning policies that can help participants in the tactical capitalising of opportunities.

Clinical Trials Speeded Up by Easy Patient Availability

New member countries offer the pharmaceutical market great potential for revenue growth with their large untapped and treatment-na・e patient base. This raises the chances for swift patient trials, particularly because treatment occurs mostly in large volume hospitals. This process of patient recruitment is highly efficient compared to trials conducted through individual physician practices. The abundance of patient volunteers allows speedy completion of clinical trials whereas over 80 per cent of the trials conducted in the West are delayed due to a dearth of volunteers.

"These rapid trials are further boosted by the easy availability of highly skilled, motivated and qualified (to MD and PhD level) investigators willing to work for lower wages than their western counterparts," observes the analyst of this research. "These investigators are also familiar with red tape issues and are highly compliant with the documentation requirements of clinical trials."

Entry Issues a Setback for Foreign Companies in New EU Market

With a patient base of over 400 million, large multi-national pharmaceuticals and biotechnologies companies are using these new EU countries for phase I, II and phase III studies. Besides lesser-known diseases, these countries also offer the opportunity to test for large global markets at relatively lowered costs. This regional advantage allows pharmaceutical companies overcome their biggest expense -- the cost incurred by way of delayed time to market.

However, local participants overshadow most multinational companies in the new EU markets. "Foreign companies and even local companies need to present compelling health economic data to justify a products price and retain premium," explains the analyst. "Further, they need to upgrade existing approval dossiers in the candidate countries in order to comply with the EU laws."

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Table of Contents

1 STRATEGIC ANALYSIS OF THE OPPORTUNITIES FOR PHARMACEUTICAL AND BIOTECHNOLOGY INDUSTRY IN THE NEW EU COUNTRIES

Overview

Research Scope and Methodology

European Union

European Union Healthcare

Challenges in the New EU Market

Opportunities in Clinical Trials

Strategic Recommendations

Industry Participants

Decision Support Databases

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