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Good documentation practice (recommended to abbreviate as GDocP to distinguish from "good distribution practice" also abbreviated GDP) is a term in the pharmaceutical and medical device industries to describe standards by which documents are created and maintained.
A key aspect of specification by example is creating a single source of truth about required changes from all perspectives. When business analysts work on their own documents, software developers maintain their own documentation and testers maintain a separate set of functional tests, software delivery effectiveness is significantly reduced by the need to constantly coordinate and synchronise ...
Good pharmacovigilance practice (GVP), for the safety of produced drugs; Good regulatory practice (GRP), for the management of regulatory commitments, procedures and documentation; Collectively, these and other good-practice requirements are referred to as "GxP" requirements, all of which follow similar philosophies. Other examples include good ...
ISO/IEC/IEEE 29119 Software and systems engineering -- Software testing [1] is a series of five international standards for software testing.First developed in 2007 [2] and released in 2013, the standard "defines vocabulary, processes, documentation, techniques, and a process assessment model for testing that can be used within any software development lifecycle."
This standardized template conforms to guidelines by the user warnings project. You may discuss the visual appearance of these standardized templates (e.g. the image in the top-left corner) at the user warning talk page. Please refer to the index of message templates before using any template on user talk pages to warn a user. Applying the best ...
Download as PDF; Printable version; ... Software test documentation; ... Template documentation. See also. IEEE standards This page was last edited on 19 ...
Good agricultural practice; Good automated manufacturing practice; Good clinical data management practice; Good clinical laboratory practice; Good clinical practice; Good Clinical Practice Directive; Good documentation practice; Good engineering practice; Good manufacturing practice; Good safety practice; Good tissue practice
Test coverage in the test plan states what requirements will be verified during what stages of the product life. Test coverage is derived from design specifications and other requirements, such as safety standards or regulatory codes, where each requirement or specification of the design ideally will have one or more corresponding means of verification.