Views from Multinational Pharmaceutical Companies on Allocation of Clinical Trials in Saudi Arabia-Qualitative Study.

IF 2 Q3 PHARMACOLOGY & PHARMACY
Pharmacy Pub Date : 2024-11-12 DOI:10.3390/pharmacy12060167
Nouf M Aloudah, Ahmed M Shaman
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引用次数: 0

Abstract

Clinical trials conducted by pharmaceutical companies are essential for bridging local research efforts with broader populations, facilitating the transfer of valuable insights and solutions. This study aimed to explore the barriers and facilitators affecting clinical trials in Saudi Arabia from the perspective of key personnel within the pharmaceutical industry and Contract Research Organizations (CROs). We conducted in-depth semi-structured interviews with nine participants, which provided a holistic understanding of the intricate dynamics shaping the landscape of clinical trials in the country. The analysis revealed three prominent themes: operational challenges, complexities in navigating approval hurdles, and the unique value proposition for conducting clinical trials in Saudi Arabia. The participants expressed pride in the local infrastructure but acknowledged existing flaws, particularly in regulatory processes that contribute to delays in trial initiation. They emphasized the importance of conducting clinical trials in areas such as diabetes, crowd management during pilgrimages, and rare diseases, which are prevalent in the region. Despite the limited number of clinical trials registered (354 from 2009 to 2020, with only 1% being phase 1 studies), Saudi Arabia's total pharmaceutical market exceeds SAR 13 billion, positioning it as the largest market in the region. Stakeholders recognized the country's potential as a research hub, particularly within the Gulf Cooperative Council (GCC) region. However, to attract more trials and enhance the medical research landscape, it is crucial to address the identified barriers, streamline processes, and improve stakeholder alignment. The findings highlight the need for targeted interventions to overcome these challenges and leverage Saudi Arabia's investments in healthcare infrastructure since its transformation program launched in 2010. By enhancing the regulatory environment and fostering collaboration among stakeholders, Saudi Arabia can solidify its role as a key player in international clinical research.

跨国制药公司对沙特阿拉伯临床试验分配的看法--定性研究。
制药公司开展的临床试验对于将本地研究工作与更广泛的人群联系起来、促进宝贵见解和解决方案的转让至关重要。本研究旨在从制药行业和合同研究组织 (CRO) 主要人员的角度,探讨影响沙特阿拉伯临床试验的障碍和促进因素。我们对九位参与者进行了深入的半结构式访谈,从而全面了解了影响该国临床试验格局的复杂动态。分析揭示了三个突出主题:运营挑战、通过审批障碍的复杂性以及在沙特阿拉伯开展临床试验的独特价值主张。与会者对当地的基础设施表示自豪,但也承认存在缺陷,特别是在监管流程方面,这导致了试验启动的延误。他们强调了在糖尿病、朝圣期间的人群管理和罕见病等领域开展临床试验的重要性,这些疾病在该地区非常普遍。尽管注册的临床试验数量有限(2009 年至 2020 年为 354 项,其中一期研究仅占 1%),但沙特阿拉伯的医药市场总额超过 130 亿沙特里亚尔,是该地区最大的市场。利益相关者认识到该国作为研究中心的潜力,尤其是在海湾合作委员会 (GCC) 地区。然而,要吸引更多试验并改善医学研究环境,关键是要解决已发现的障碍、简化流程并改善利益相关者之间的协调。研究结果突出表明,需要采取有针对性的干预措施来克服这些挑战,并充分利用沙特阿拉伯自 2010 年启动转型计划以来在医疗保健基础设施方面的投资。通过加强监管环境和促进利益相关者之间的合作,沙特阿拉伯可以巩固其在国际临床研究中的重要地位。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Pharmacy
Pharmacy PHARMACOLOGY & PHARMACY-
自引率
9.10%
发文量
141
审稿时长
11 weeks
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