Strengthening the Application of the DAIDS GCLP Guidelines: The Implementation of an Integrated Laboratory Oversight Framework

被引:0
|
作者
Nguyen, Loc [1 ]
Leach, Anne [2 ]
Piwowar-Manning, Estelle [3 ]
Marzinke, Mark [3 ]
Levesque, Allan [4 ]
Gregorio, Claudine [4 ]
Skinner, Kristen [5 ,6 ]
Towindo, Tiri [1 ]
Hanes, Heidi [2 ]
Sarpong, Kwabena [7 ]
Kasongo, Christian [8 ]
Samsunder, Natasha [9 ]
Aldrovandi, Grace [10 ]
Ferbas, Kathie G. [10 ]
Engelbrecht, Andries [11 ]
Stirewalt, Michael [11 ,15 ]
Anyango, Emily [12 ]
Ubolyam, Sasiwimol [13 ]
Lankford-Turner, Pamela [14 ]
Sarzotti-Kelsoe, Marcella [2 ]
机构
[1] PPD, Thermo Fisher Sci, Wilmington, NC USA
[2] Johns Hopkins Univ, Dept Pathol, Patient Safety Monitoring Int Labs pSMILE, Baltimore, MD USA
[3] Johns Hopkins Univ, Dept Pathol, HIV Prevent Trials Network LC, Baltimore, MD USA
[4] Westat Corp, Rockville, MD USA
[5] Duke Univ, Med Ctr, Dept Surg, Durham, NC USA
[6] Duke Univ, Ctr AIDS Res, Med Ctr, Durham, NC USA
[7] Infect Dis Inst IDI, Core Lab, Kampala, Uganda
[8] Aurum Inst, Johannesburg, South Africa
[9] Ctr AIDS Programme Res South Africa CAPRISA, Berea, South Africa
[10] Univ Calif Los Angeles, Int Maternal Pediat Adolescent AIDS Clin Trials &, Los Angeles, CA USA
[11] HIV Vaccine Trials Network LC, Cape Town, South Africa
[12] Kenya Govt Med Res Ctr, Nairobi, Kenya
[13] HIV Netherlands Australia Thailand HIV NAT AIDS Re, Bangkok, Thailand
[14] Emory Infect Dis Clin Res Lab, Decatur, GA USA
[15] HIV Vaccine Trials Network LC, Seattle, WA USA
关键词
Clinical Trials; Collaboration; DAIDS GCLP Guidelines; GCLP training; GCLP audit; Laboratory Quality Improvement; PROFICIENCY TESTING PROGRAM; QUALITY-ASSURANCE PROGRAM;
D O I
10.1089/aid.2024.0042
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The Division of AIDS (DAIDS) Good Clinical Laboratory Practice (GCLP) Guidelines establish a framework to guide the oversight of laboratories supporting DAIDS-sponsored clinical research or trials. Compliance with these guidelines promotes data reliability, validity, and safety of the clinical research or trial participants and laboratory staff and ensures adherence to regulatory requirements. Acknowledgment and adoption of the DAIDS GCLP Guidelines are critical in building laboratory capacity and preparedness for conducting clinical trials. In collaboration with DAIDS, laboratory experts support the implementation of the DAIDS Integrated Laboratory Oversight Framework (Framework) activities. This article describes the implementation of the GCLP Guidelines, the Framework activities, and the coordinated efforts to strengthen laboratory performance. The Framework activities include four components: Quality Assurance Oversight, GCLP Audits, GCLP Training, and Laboratory Quality Improvement. Comparison of GCLP Guidelines with other regulations or standards, including U.S. Clinical Laboratory Improvement Amendments regulation 42 CFR 493, College of American Pathologists, World Health Organization GCLP, and International Organization for Standardization, ISO 15189:2012 standards, highlighted the differences and similarities to guide integration and harmonization efforts. Processes related to the Framework activities are outlined in detail, including key data derived from the managed activities of over 175 laboratories worldwide. Via the evolution of the DAIDS GCLP Guidelines and laboratory oversight workflows, the laboratories participating in DAIDS-sponsored clinical research and trials have successfully participated in internal and external regulatory audits. The collaborative and integrated oversight approach promotes knowledge-sharing and accountability to support the implementation of the DAIDS GCLP Guidelines and compliance monitoring. Lessons learned have helped with the implementation of the DAIDS integrated laboratory oversight approach and quality oversight programs at multiple laboratories worldwide.
引用
收藏
页码:622 / 630
页数:9
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