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