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From Wikipedia, the free encyclopedia

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.

A "c" or "C" is sometimes added to the front of the initialism. The preceding "c" stands for "current." For example, cGMP is an acronym for "current good manufacturing practice". The term GxP is frequently used to refer in a general way to a collection of quality guidelines.[1]

Purpose

The purpose of the GxP quality guidelines is to ensure a product is safe and meets its intended use. GxP guides quality manufacture in regulated industries including food, drugs, medical devices and cosmetics.

The most central aspects of GxP are Good Documentation Practices (GDP), which are expected to be ALCOA:

  • Attributable: documents are attributable to an individual
  • Legible: they are readable
  • Contemporaneously Recorded: not dated in the past or the future, but when the documented task is completed
  • Original or a True Copy
  • Accurate: accurately reflecting the activity documented
  • and Permanent,

The products that are the subject of the GxP are expected to be

  • Traceability: the ability to reconstruct the development history of a drug or medical device.
  • Accountability: the ability to resolve who has contributed what to the development and when.

GxPs require that a Quality System be established, implemented, documented, and maintained.

As explained above, documentation is a critical tool for ensuring GxP adherence. For more information, see good manufacturing practice.

Examples of GxPs

See also

References

  1. ^ ISPE - GAMP® Good Practice Guide: A Risk-Based Approach to GxP Compliant Laboratory Computerized Systems
  2. ^ United States Environmental Protection Agency (1995). "Good Automated Laboratory Practices - Principles and Guidance to Regulations for Ensuring Data Integrity in Automated Laboratory Operations". U.S. EPA, Office of Information Resources Management. Retrieved 25 February 2012.
  3. ^ K., Nitahara (March–June 1993). "Good Automated Laboratory Practices and other standards: validation of computer systems in the PC environment". Qual Assur. 2 (1–2): 96–101. PMID 8156229.
  4. ^ Coecke S. "Guidance on Good Cell Culture Practice".
  5. ^ Food and Drug Administration (2000). "Administrative Practices and Procedures; Good Guidance Practices". Archived from the original on 18 January 2009. Retrieved 10 April 2009.
  6. ^ Food and Drug Administration. "Good Guidance Practices (GGP) Database". Archived from the original on 30 March 2009. Retrieved 10 April 2009.
This page was last edited on 17 January 2021, at 12:29
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