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Disposable Injection Devices - Products, Players and Prospects
Greystone Associates, Feb 2007, Pages: 110
Because they cannot tolerate the first-pass metabolism of the digestive tract, the recent escalation in new biological drugs, including antibodies and recombinant proteins, is placing renewed emphasis on drug injection. Now a number of factors are converging to create both risk and opportunity for parenteral drug makers and their device partners. These include new classes of drugs for previously refractory conditions, the growing trend toward self-administration for chronic diseases, shifting patient demographics in industrial countries, caregiver safety legislation, and continued pressure to control healthcare costs. These factors are giving rise to a new generation of sophisticated, application-specific disposable injection devices designed to satisfy caregiver and patient preferences while addressing managed care initiatives and the limitations of new classes of therapeutic drugs. Because of their ability to safety and reliably satisfy treatment protocols and compliance goals, these new devices will have a significant impact on the future of patient care.
Market Data
The study presents qualitative and quantitative data and information on key market measures and benchmarks:
- Market Size by Segment
- Economic Factors
- Company Profiles
- Injector Design Criteria
- Product Status & Prospects
- Market Projections
- Industry Structure
- Strategic Alliances
- Cost & Pricing Factors
- Proprietary Technology
- Emerging Markets
- Market Penetration Factors
- Technology Factors
- Regulatory Factors
Feature Summary
-Analyzes and evaluates the new generation of disposable injection devices and assesses the market potential for existing and probable future devices
-Analyzes product designs, technologies and market development issues
-Provides detailed descriptions of disposable device market drivers, design approaches, and business strategies
-Forecasts device usage 2010
-Profiles disposable injector companies, their product development activities, business strategies, and corporate alliances and affiliations
-Evaluates the impact of economic, technology, and regulatory factors on parenteral drug delivery markets
Report Format and Availability
This report is available in hard copy or electronic format. A site license for a single physical location and a global license are also available
Methodology:
Research methodology is based on primary research in the form of in-depth interviews with key market participants, technology developers, distributors, industry experts, and market influencers, a list that includes regulatory officials, industry trade groups, and materials standards organizations.
Primary data is evaluated and normalized against secondary sources including trade journal articles, technical literature, industry publications, company data sheets and published information, and statistical data from government agencies and trade associations.
Forecasts and projections of market demand and future market activity are derived using standard modeling and statistical techniques
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