Scientific and Regulatory Policy Committee (SRPC) Paper: Validation of Digital Pathology Systems in the Regulated Nonclinical Environment. (January 2013)

• Record Type: Journal Article
• Authors: Long, Richard E.; Smith, Adam; Machotka, Sam V.; Chlipala, Elizabeth; Cann, Jennifer; Knight, Brian; Kawano, Yoshihiro; Ellin, Jesus; Lowe, Amanda
• Is Part Of: Toxicologic pathology. Volume 41:Number 1(2013)
• Page Start: 115
• Page End: 124
• Publication Date: 2013-01
• Subjects: validation -- digital pathology systems -- whole slide scanner -- nonclinical -- computerized systems.; Pathology -- Periodicals; Toxicology -- Periodicals; Pathology; Toxicology; 615.9
• DOI: 10.1177/0192623312451162
• Languages: English
• ISSNs: 0192-6233

Abstract

Digital Pathology Systems (DPS) are dynamic, image-based computer systems that enable the acquisition, management, and interpretation of pathology information generated from digitized glass slides. This article provides a roadmap for (1) qualification of a whole slide scanner (WSS) during a validation project, (2) validation of software required to generate the whole slide image (WSI), and (3) an introduction to visual digital image evaluation and image analysis. It describes a validation approach that can be utilized when validating a DPS. It is not the intent of this article to provide guidance on when validation of DPS is required. Rather, the article focuses on technical aspects of validation of the WSS system (WSS, IT infrastructure, and associated software) portion of a DPS and covers the processes of setting up the WSS for scanning a glass slide through saving a WSI on a server. Validation of a computerized system, such as a DPS, for use in a regulated nonclinical environment is governed by Code of Federal Regulations (CFR) Title 21 part 11: Electronic Records; Electronic Signature and predicate rules associated with Good Laboratory Practices documents including 21 CFR part 58. Similar regulation and predicate rules apply in the European Union and Japan.