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Clinical Research Environment in India: Challenges and Proposed Solutions.

机译:印度的临床研究环境:挑战和提出的解决方案。

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摘要

India has compelling need and keen aspirations for indigenous clinical research. Notwithstanding this need and previously reported growth the expected expansion of Indian clinical research has not materialized. We reviewed the scientific literature, lay press reports, and ClinicalTrials.gov data for information and commentary on projections, progress, and impediments associated with clinical trials in India. We also propose targeted solutions to identified challenges. The Indian clinical trial sector grew by (+) 20.3% CAGR (compound annual growth rate) between 2005 and 2010 and contracted by (-) 14.6% CAGR between 2010 and 2013. Phase-1 trials grew by (+) 43.5% CAGR from 2005-2013, phase-2 trials grew by (+) 19.8% CAGR from 2005-2009 and contracted by (-) 12.6% CAGR from 2009-2013, and phase-3 trials grew by (+) 13.0% CAGR from 2005-2010 and contracted by (-) 28.8% CAGR from 2010-2013. This was associated with a slowing of the regulatory approval process, increased media coverage and activist engagement, and accelerated development of regulatory guidelines and recuperative initiatives. We propose the following as potential targets for restorative interventions: Regulatory overhaul (leadership and enforcement of regulations, resolution of ambiguity in regulations, staffing, training, guidelines, and ethical principles [e.g., compensation]).Education and training of research professionals, clinicians, and regulators.Public awareness and empowerment. After a peak in 2009-2010, the clinical research sector in India appears to be experiencing a contraction. There are indications of challenges in regulatory enforcement of guidelines; training of clinical research professionals; and awareness, participation, partnership, and the general image amongst the non-professional media and public. Preventative and corrective principles and interventions are outlined with the goal of realizing the clinical research potential in India.
机译:印度对本土临床研究有迫切的需求和强烈的愿望。尽管有这种需求并且以前有报道,印度临床研究的预期扩展尚未实现。我们审查了科学文献,新闻报道和ClinicalTrials.gov数据,以获取有关印度临床试验相关的预测,进展和障碍的信息和评论。我们还针对已发现的挑战提出有针对性的解决方案。印度临床试验部门在2005年至2010年之间以(+)20.3%的复合年增长率增长,在2010年至2013年之间以(-)14.6%的复合年增长率收缩。第一阶段试验的增长率为(+)43.5%, 2005-2013年,第二阶段试验从2005-2009年以(+)CAGR增长,而从2009-2013年以(-)12.6%CAGR收缩,而第三阶段试验从2005-2009年以(+)13.0%CAGR增长2010年并从2010-2013年以(-)28.8%的复合年增长率收缩。这与监管审批过程的放慢,媒体报道的增加和激进主义者的参与以及监管准则和康复计划的加速发展有关。我们提出以下作为恢复性干预措施的潜在目标:监管改革(领导和法规执行,解决法规,服务人员,培训,指南和道德原则(例如,补偿)等模棱两可的问题)。研究专业人员,临床医生的教育和培训以及监管机构。公众意识和授权。在2009年至2010年达到顶峰之后,印度的临床研究部门似乎正在萎缩。有迹象表明,准则的监管执行存在挑战;培训临床研究专业人员;非专业媒体和公众之间的意识,参与,伙伴关系和总体形象。概述了预防和纠正原则与干预措施,旨在实现印度的临床研究潜力。

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