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	<title>Good engineering practice - Revision history</title>
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	<updated>2026-05-07T15:35:07Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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		<id>http://debianws.lexgopc.com/wiki143/index.php?title=Good_engineering_practice&amp;diff=3711365&amp;oldid=prev</id>
		<title>imported&gt;Chongkian: write common abbreviations (as an alternative name) in bold and parentheses per MOS:BOLDALTNAMES</title>
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		<updated>2024-02-06T13:50:35Z</updated>

		<summary type="html">&lt;p&gt;write common abbreviations (as an alternative name) in bold and parentheses per &lt;a href=&quot;/wiki143/index.php?title=MOS:BOLDALTNAMES&amp;amp;action=edit&amp;amp;redlink=1&quot; class=&quot;new&quot; title=&quot;MOS:BOLDALTNAMES (page does not exist)&quot;&gt;MOS:BOLDALTNAMES&lt;/a&gt;&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;&amp;#039;&amp;#039;&amp;#039;Good engineering practice&amp;#039;&amp;#039;&amp;#039; (&amp;#039;&amp;#039;&amp;#039;GEP&amp;#039;&amp;#039;&amp;#039;) 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 requirements for qualification or validation. Good engineering practices are applied to all industries that require engineering.&amp;lt;ref&amp;gt;{{Cite web|title=Good Practice Guide: Good Engineering Practice|url=https://ispe.org/publications/guidance-documents/good-practice-guide-good-engineering-practice|access-date=2020-09-12|website=ISPE {{!}} International Society for Pharmaceutical Engineering|language=en}}&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==See also==&lt;br /&gt;
* [[GxP]]&lt;br /&gt;
* [[Good manufacturing practice]] (GMP)&lt;br /&gt;
* [[Best practice]]&lt;br /&gt;
* [[American National Standards Institute]] (ANSI)&lt;br /&gt;
* [[Institute of Electrical and Electronics Engineers]] (IEEE)&lt;br /&gt;
* [[European Medicines Agency]] (EMEA)&lt;br /&gt;
* [[Food and Drug Administration]] (FDA)&lt;br /&gt;
* [[Ministry of Health, Labour and Welfare (Japan)]]&lt;br /&gt;
* [[Pharmaceutical Inspection Convention and Pharmaceutical Inspection Co-operation Scheme]] (PIC/S)&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
{{Reflist}}&lt;br /&gt;
&lt;br /&gt;
==Sources==&lt;br /&gt;
* [https://web.archive.org/web/20110929185235/http://www.ispe.org/galleries/reg-new-gallery/Qualfor21stCentury.pdf Risk-Based Qualification for the 21st Century]&lt;br /&gt;
* [https://web.archive.org/web/20080302115658/http://www.ispe.org/page.ww?name=Welcome+to+the+ISPE+GAMP+COP&amp;amp;section=GAMP+COP ISPE GAMP COP]&lt;br /&gt;
&lt;br /&gt;
[[Category:Quality|Good]]&lt;br /&gt;
[[Category:Engineering concepts]]&lt;br /&gt;
[[Category:Good practice]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{engineering-stub}}&lt;/div&gt;</summary>
		<author><name>imported&gt;Chongkian</name></author>
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