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该国临床研究标准化、质量及伦理监督的现状:对中央药品标准控制组织(伦理委员会注册)及医院和医疗服务提供者国家认证委员会(认证)数据库的审计

Current status of standardized, quality and ethical oversight of clinical research in the country: An audit of the Central Drugs Standard Control Organization (registration of ethics committees) and national accreditation board for hospital and healthcare providers (accreditation) databases.

作者信息

Nishandar Tushar Bhimrao, Birajdar Amit Ravindra, Gogtay Nithya J, Thatte Urmila M

机构信息

Department of Clinical Pharmacology, Seth G S Medical College and KEM Hospital, Mumbai, Maharashtra, India.

出版信息

Perspect Clin Res. 2019 Apr-Jun;10(2):84-90. doi: 10.4103/picr.PICR_93_18.

DOI:10.4103/picr.PICR_93_18
PMID:31008075
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6463500/
Abstract

PURPOSE

The Prof. Ranjit Roy Chaudhury committee report recommended the accreditation of Institutional Ethics Committees (IECs). Rule 122DD of the Drugs and Cosmetics Act (and Rules) mandates that only registered ECs can accord approval for regulatory studies. We evaluated the current status of registered, reregistered, and accredited ECs in the country to assess the impact of both the recommendation and rule.

MATERIALS AND METHODS

Websites of stakeholders-the Central Drugs Standard Control Organization (CDSCO), National Accreditation Board for Hospitals and Healthcare Providers (NABH) were assessed. Information on registration status was then compared with regulatory clinical trials in the Clinical Trials Registry of India, population demographics of all states, and the Medical Council of India recognized postgraduate medical colleges in the various states.

RESULTS

A total of 1268 ECs were registered with CDSCO. Of these, 1008 (79.5%) were institutional and 256 (20.18%) independent ECs. A total of 499/1268 (39.4%) ECs were reregistered. Of which 449/499 (90%) were institutional and 50/499 (10%) were independent. Institutional ECs were five times more likely to be reregistered with CDSCO relative to independent ECs (cOR 4.52 [3.12, 6.54], < 0.0001). A total of 15/233 (7%) applications to NABH had received accreditation. A wide skew was seen in the distribution of ECs across various states as also their oversight of regulatory clinical trials.

CONCLUSIONS

Registration and reregistration of ECs along with accreditation is not commensurate with the needs of the country at this time and must be vigorously promoted.

摘要

目的

兰吉特·罗伊·乔杜里教授委员会的报告建议对机构伦理委员会(IEC)进行认证。《药品和化妆品法案》(及规则)第122DD条规定,只有注册的伦理委员会才能批准监管研究。我们评估了该国注册、重新注册和获得认证的伦理委员会的现状,以评估该建议和规则的影响。

材料与方法

评估了利益相关者的网站——中央药品标准控制组织(CDSCO)、医院和医疗服务提供者国家认证委员会(NABH)。然后将注册状态信息与印度临床试验注册中心的监管临床试验、所有邦的人口统计数据以及印度医学委员会认可的各邦研究生医学院进行比较。

结果

共有1268个伦理委员会在CDSCO注册。其中,1008个(79.5%)是机构伦理委员会,256个(20.18%)是独立伦理委员会。共有499/1268(39.4%)个伦理委员会进行了重新注册。其中449/499(90%)是机构伦理委员会,50/499(10%)是独立伦理委员会。相对于独立伦理委员会,机构伦理委员会在CDSCO重新注册的可能性是其五倍(校正比值比4.52 [3.12, 6.54],<0.0001)。向NABH提交的233份申请中,共有15份(7%)获得了认证。伦理委员会在各邦的分布及其对监管临床试验的监督存在很大偏差。

结论

目前伦理委员会的注册、重新注册以及认证与该国的需求不相称,必须大力推动。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7829/6463500/71af2702b1b0/PCR-10-84-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7829/6463500/ef0934a4b7e1/PCR-10-84-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7829/6463500/e0f664c5e0c7/PCR-10-84-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7829/6463500/71af2702b1b0/PCR-10-84-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7829/6463500/ef0934a4b7e1/PCR-10-84-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7829/6463500/e0f664c5e0c7/PCR-10-84-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7829/6463500/71af2702b1b0/PCR-10-84-g003.jpg

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