Talk:Good practice

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Hi, I wrote this page based on a short but inspiring mission in the pharma industry. I have an IT background; could anyone with a more solid understanding of this topic do a review of the content? Thx, Hans

GIP for IT topics in GxP

Hans,

Thanks for posting this GxP page. I have a suggestion: I would like to add GIP for Good Information Practices to the list. Then we could move and expand your IT discussion to a new GIP page, and expand the General GxP introduction. Disclaimer: I am a volunteer on a project (LSIT) to write and formalize GIP. Jmcneil86043 16:42, 16 March 2007 (UTC)[reply]

I've just read your comment.
At least in a pharmaceutical context, GxP jointly refers to the regulated good practices exclusively; i.e. (in alphabetical order) :
GCP - Good Clinical Practice
GDP - Good Distribution Practice
GLP - (preclinical) Good Laboratory Practice
GMP - Good Manufacturing Practice
GQP - Good Quality Practice (in Japan)
GVP - Good Vigilance Practice (in Europe)
In addition, QS - Quality System (practices) and RA - Regulatory Affairs (practices) could be considered being part of the pharmaceutical GxP framework; likewise for the medical device related Quality System (see 21CFR820: Quality System Regulation (QSR/QMSR).
Good information/IT practices), good business practices, etc. are not regulated and, as such, they are not part of the pharmaceutical GxP framework.
Since the pharmaceutical agencies are currently working on AI implementation within a pharmaceutical and medical devices context, we should maybe consider in the future to extend GxP to GMLP - Good Machine Learning Practice - if binding regulatory texts are issued about this topic. 2A01:E0A:2ED:11F0:742E:5463:D6DA:EBB9 (talk) 13:21, 8 March 2025 (UTC)[reply]

A topic of ....

Good hospital practice has been added based on the following http://scholar.google.com/scholar?q=allintitle:+good+hospital+practice&hl=en&lr=&newwindow=1&start=0&sa=N --222.67.207.79 (talk) 08:34, 2 July 2009 (UTC)[reply]

Info about the topic of .....

--222.67.215.129 (talk) 02:25, 18 June 2010 (UTC)[reply]

GxP in regulated environment .....

GxP is a term used initially for regulated environment to indicate all law and regulations (e.g. Code of Federal Regulation) applicable to Pharmaceutical: Good Laboratory/Clinical/Manufacturing/Distribution Practice. The term should not be applied to guideline or similar documentation issued to standardize a good working practice: e.g. GAMP, GIP, GEP, GHP, etc. For that you should specify the specific acronym.

198.28.69.5 (talk) 13:01, 4 May 2011 (UTC)[reply]

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GAMP is no longer an abbreviation for Good Automated Manufacturing Practice

ISPE has registered GAMP as a trademark and no longer uses GAMP as an abbreviation. See: https://ispe.org/pharmaceutical-engineering/january-february-2025/celebrating-25-years-gampr-americas. This is intended to emphasize that the GAMP guidance applies across all GxP areas within the life sciences sector. I would remove GAMP from this list… PassionateGAMPer (talk) 08:38, 24 November 2025 (UTC)[reply]

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