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相似文献

1
Sound practices for consistent human visual inspection.一致的人类视觉检查的良好实践。
AAPS PharmSciTech. 2011 Mar;12(1):215-21. doi: 10.1208/s12249-010-9577-7. Epub 2011 Jan 4.
2
The scientific basis for visible particle inspection.可见异物检查的科学依据。
PDA J Pharm Sci Technol. 1999 Nov-Dec;53(6):291-302.
3
[Pharmaceutical product quality control and good manufacturing practices].[药品质量控制与良好生产规范]
Kokuritsu Iyakuhin Shokuhin Eisei Kenkyusho Hokoku. 2010(128):1-16.
4
WHO Expert Committee on Specifications for Pharmaceutical Preparations. Fiftieth report.世界卫生组织药物制剂规范专家委员会。第五十次报告。
World Health Organ Tech Rep Ser. 2016(996):1-358, back cover.
5
Rationale drug therapy: reasons for failure and suggestions for its implementation.合理药物治疗:失败原因及其实施建议。
Indian Pediatr. 1993 Jun;30(6):815-8.
6
Automated particulate inspection systems: strategies and implications.自动化颗粒检测系统:策略与影响
J Parenter Sci Technol. 1990 Mar-Apr;44(2):74-107.
7
Considerations for design and use of container challenge sets for qualification and validation of visible particulate inspection.用于可见微粒检查的确认和验证的容器挑战装置的设计和使用考量。
PDA J Pharm Sci Technol. 2012 May-Jun;66(3):273-84. doi: 10.5731/pdajpst.2012.00862.
8
Literature Abstracts.文献摘要
J Texture Stud. 1971 May;2(2):249-256. doi: 10.1111/j.1745-4603.1971.tb00588.x.
9
Drug quality control work in Daru: observations during 1983-1986.达鲁的药品质量控制工作:1983 - 1986年期间的观察
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Dynamic Image Analysis To Evaluate Subvisible Particles During Continuous Drug Infusion In a Neonatal Intensive Care Unit.动态图像分析在新生儿重症监护病房连续药物输注过程中评估亚可见颗粒。
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Possible Incompatibility between Amino Acids and Copper in Solutions for Pediatric Parenteral Nutrition.小儿肠外营养溶液中氨基酸与铜之间可能存在的不相容性。
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本文引用的文献

1
The scientific basis for visible particle inspection.可见异物检查的科学依据。
PDA J Pharm Sci Technol. 1999 Nov-Dec;53(6):291-302.
2
Points to consider for cleaning validation. Technical Report No. 29. PDA. Parental Drug Association.清洁验证需考虑的要点。技术报告第29号。PDA(注射剂药物协会)
PDA J Pharm Sci Technol. 1998;52(6 Suppl):1-23.
3
Particulate inspection of parenteral products: an assessment.注射用药品的微粒检查:一项评估。
J Parenter Sci Technol. 1981 Jul-Aug;35(4):176-85.
4
Generalized methodology for evaluation of parenteral inspection procedures.肠胃外检查程序评估的通用方法。
J Parenter Drug Assoc. 1980 Jan-Feb;34(1):14-61.
5
Inventory and measurement of particulates in sealed sterile containers.密封无菌容器中微粒的清点与测量
J Parenter Sci Technol. 1983 Sep-Oct;37(5):170-9.
6
Standard particulate sets for visual inspection systems: their preparation, evaluation, and applications.视觉检测系统的标准颗粒集:其制备、评估及应用
J Parenter Sci Technol. 1986 Nov-Dec;40(6):265-76.
7
Particulate matter in parenteral products: a review.注射用产品中的颗粒物:综述
J Parenter Sci Technol. 1986 Sep-Oct;40(5):212-41.
8
Automated particulate inspection systems: strategies and implications.自动化颗粒检测系统:策略与影响
J Parenter Sci Technol. 1990 Mar-Apr;44(2):74-107.

一致的人类视觉检查的良好实践。

Sound practices for consistent human visual inspection.

出版信息

AAPS PharmSciTech. 2011 Mar;12(1):215-21. doi: 10.1208/s12249-010-9577-7. Epub 2011 Jan 4.

DOI:10.1208/s12249-010-9577-7
PMID:21203872
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3066354/
Abstract

Numerous presentations and articles on manual inspection of pharmaceutical drug products have been released, since the pioneering articles on inspection by Knapp and associates Knapp and Kushner (J Parenter Drug Assoc 34:14, 1980); Knapp and Kushner (Bull Parenter Drug Assoc 34:369, 1980); Knapp and Kushner (J Parenter Sci Technol 35:176, 1981); Knapp and Kushner (J Parenter Sci Technol 37:170, 1983). This original work by Knapp and associates provided the industry with a statistical means of evaluating inspection performance. This methodology enabled measurement of individual inspector performance, performance of the entire inspector pool and provided basic suggestions for the conduct of manual inspection. Since that time, numerous subject matter experts (SMEs) have presented additional valuable information for the conduct of manual inspection Borchert et al. (J Parenter Sci Technol 40:212, 1986); Knapp and Abramson (J Parenter Sci Technol 44:74, 1990); Shabushnig et al. (1994); Knapp (1999); Knapp (2005); Cherris (2005); Budd (2005); Barber and Thomas (2005); Knapp (2005); Melchore (2007); Leversee and Ronald (2007); Melchore (2009); Budd (2007); Borchert et al. (1986); Berdovich (2005); Berdovich (2007); Knapp (2007); Leversee and Shabushing (2009); Budd (2009). Despite this abundance of knowledge, neither government regulations nor the multiple compendia provide more than minimal guidance or agreement for the conduct of manual inspection. One has to search the literature for useful information that has been published by SMEs in the field of Inspection. The purpose of this article is to restate the sound principles proclaimed by SMEs with the hope that they serve as a useful guideline to bring greater consistency to the conduct of manual inspection.

摘要

已经发布了许多关于药品人工检查的演讲和文章,这些文章源于 Knapp 及其同事的开创性研究:Knapp 和 Kushner(J Parenter Drug Assoc 34:14, 1980);Knapp 和 Kushner(Bull Parenter Drug Assoc 34:369, 1980);Knapp 和 Kushner(J Parenter Sci Technol 35:176, 1981);Knapp 和 Kushner(J Parenter Sci Technol 37:170, 1983)。Knapp 及其同事的这项开创性工作为行业提供了一种评估检查性能的统计方法。该方法能够衡量单个检查员的绩效、整个检查员队伍的绩效,并为人工检查的实施提供基本建议。从那时起,许多主题专家(SME)为人工检查的实施提供了更多有价值的信息,如 Borchert 等人(J Parenter Sci Technol 40:212, 1986);Knapp 和 Abramson(J Parenter Sci Technol 44:74, 1990);Shabushnig 等人(1994);Knapp(1999);Knapp(2005);Cherris(2005);Budd(2005);Barber 和 Thomas(2005);Knapp(2005);Melchore(2007);Leversee 和 Ronald(2007);Melchore(2009);Budd(2007);Borchert 等人(1986);Berdovich(2005);Berdovich(2007);Knapp(2007);Leversee 和 Shabushing(2009);Budd(2009)。尽管有如此丰富的知识,但政府法规和多个药典都没有为人工检查的实施提供更多的指导或协议。人们不得不从文献中寻找由该领域的 SME 发布的有用信息。本文的目的是重申 SME 提出的合理原则,希望这些原则能够成为一个有用的指导方针,为人工检查的实施带来更大的一致性。