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Clinical programs at biopharmaceutical organizations are increasingly looking to less expensive and regulated areas of the world to perform clinical trial activities. Emerging markets are also fast-growing regions that present future growth opportunities for organizations that have seen sales growth slow in mature markets.
However, there are still questions around the cost, quality and pitfalls of conducting clinical trials in emerging regions.
Best Practices®, LLC conducted this study to inform clinical affairs leaders at biopharma companies on benchmarks around budgets, and staffing. In addition, the study presents benchmarks and insights around the current level of clinical trials in emerging areas, the cost and quality of outside-U.S. trials, and outsourcing levels for key clinical activities.
Critical outsourcing questions addressed in this survey include:
Research participants included 7 executives and managers from 6 pharmaceuticalcompanies across a wide variety of therapeutic areas and product classes. In addition, four in-depth interviews were conducted to capture innovative practices in clinical activities in emerging areas.
Health Care; Pharmaceutical; Biotech; Medical Device
Eisai; Abbott Laboratories; Daiichi Sankyo; CSL Behring; Roche; MerckSerono