Home > Blossary: 21 CFR Part 11 -- Electronic Records and Electronic Signatures
Terms used in the Food and Drug Administration's (FDA’s) guidance on principles and procedures for creating, modifying, maintaining, archiving, retrieving, and transmitting electronic records and electronic signatures under the requirements of Part 11 of Title 21 of the Code of Federal Regulations; Electronic Records; Electronic Signatures. Many life science businesses (pharmaceutical and medical devices companies) are subject to the rule and must comply with the regulation.
Category: Health
11 Terms
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Created by: nicktruth
Number of Blossarys: 1
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A generally available software component for which the user can not claim complete software life cycle control.
Domain: Life Sciences; Category: Regulatory
Any requirements set forth in the Act (Federal Food, Drug and Cosmetic Act), the PHS Act (Public Health Service Act), or any FDA regulation (GxP: GLP, GMP, GCP, etc.), with the exception of part 11. ...
Domain: Life Sciences; Category: Regulatory
A software verification and validation task to determine the extent of verification and validation analysis and testing that must be repeated when changes are made to any previously examined software ...
Domain: Life Sciences; Category: Regulatory
The ability of a system or component to perform its required functions under stated conditions for a specified period of time.
Domain: Life Sciences; Category: Regulatory
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