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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.
Photographic documentation is usually more detailed for single-item treatments than for batch treatments. [70] A trained conservator can observe past treatments done on the book or document, but good documentation specifies the exact techniques and materials used. [71] Historically, there was no codified set of rules for book and paper ...
GxP is a general abbreviation for the "good practice" quality guidelines and regulations. The "x" stands for the various fields, including the pharmaceutical and food industries , for example good agricultural practice , or GAP.
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
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 ...
This category contains articles and categories related to the pharmaceutical industry, which consists of methods, processes, regulations, standards, and companies engaged in the development of pharmaceuticals for use in man.
Good engineering practice (GEP) is engineering and technical activities that ensure that a company manufactures products of the required quality as expected (e.g., by the relevant regulatory authorities). Good engineering practices are to ensure that the development and/or manufacturing effort consistently generates deliverables that support ...
The Principles of Good Laboratory Practice (GLP) establish rules and criteria for a quality system that oversees the organizational processes and conditions in which non-clinical health and environmental safety studies are planned, conducted, monitored, recorded, reported, and archived.