Property:Modification date

"Modification date" is a predefined property that corresponds to the date of the last modification of a subject and is provided by Semantic MediaWiki. This property is pre-deployed (also known as special property) and comes with additional administrative privileges but can be used just like any other user-defined property.

Usage1768

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Filter<p>The <a rel="nofollow" class="external text" href="https://www.semantic-mediawiki.org/wiki/Help:Property_page/Filter">search filter</a> allows the inclusion of <a rel="nofollow" class="external text" href="https://www.semantic-mediawiki.org/wiki/Help:Query_expressions">query expressions</a> such as <code>~</code> or <code>!</code>. The selected <a rel="nofollow" class="external text" href="https://www.semantic-mediawiki.org/wiki/Query_engine">query engine</a> might also support case insensitive matching or other short expressions like:</p><ul><li><code>in:</code> result should include the term, e.g. '<code>in:Foo</code>'</li></ul><ul><li><code>not:</code> result should to not include the term, e.g. '<code>not:Bar</code>'</li></ul>

Showing 20 pages using this property.

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USA Acceptance of Clinical Data to Support Medical Device Applications and Submissions Frequently Asked Questions - Guidance for Industry and Food and Drug Administration Staff 21-Feb-2018 +

12:15:27, 16 July 2026  +

USA Acceptance of Clinical Data to Support Medical Device Applications and Submissions Frequently Asked Questions - Guidance for Industry and Food and Drug Administration Staff 21-Feb-2018 - +

11:49:30, 16 July 2026  +

USA CTCAE - Common Terminology Criteria for Adverse Events v5.0 (2017) +

12:15:27, 16 July 2026  +

USA CTCAE - Common Terminology Criteria for Adverse Events v5.0 (2017) - +

11:50:13, 16 July 2026  +

USA Expedited Review: Categories of Research that may be Reviewed Through an Expedited Review Procedure 1998 +

12:15:27, 16 July 2026  +

USA Expedited Review: Categories of Research that may be Reviewed Through an Expedited Review Procedure 1998 - +

11:49:28, 16 July 2026  +

USA FD&C Act - Federal Food, Drug, and Cosmetic Act 30-Sep-2023 +

12:15:27, 16 July 2026  +

USA FD&C Act - Federal Food, Drug, and Cosmetic Act 30-Sep-2023 Sec 510 (k) +

11:49:29, 16 July 2026  +

USA FD&C Act - Federal Food, Drug, and Cosmetic Act 30-Sep-2023 Sec 512 (f) +

11:49:29, 16 July 2026  +

USA FD&C Act - Federal Food, Drug, and Cosmetic Act 30-Sep-2023 Sec 737 (8) +

11:49:29, 16 July 2026  +

USA FD&C Act - Federal Food, Drug, and Cosmetic Act 30-Sep-2023 Section 513 +

11:49:29, 16 July 2026  +

USA FDA - E6(R2) Good Clinical Practice: Integrated Addendum to ICH E6(R1): Guidance for Industry March 2018 +

12:15:27, 16 July 2026  +

USA FDA - E6(R2) Good Clinical Practice: Integrated Addendum to ICH E6(R1): Guidance for Industry March 2018 - +

11:49:30, 16 July 2026  +

USA FDA - HUMAN DRUG CGMP NOTES Volume 8, Number 3 +

12:15:27, 16 July 2026  +

USA FDA - HUMAN DRUG CGMP NOTES Volume 8, Number 3 6 +

11:50:08, 16 July 2026  +

USA FDA Guidance for Clinical Investigators, Sponsors, and IRBs Adverse Event Reporting to IRBs — Improving Human Subject Protection Jan-2009 +

12:15:27, 16 July 2026  +

USA FDA Guidance for Clinical Investigators, Sponsors, and IRBs Adverse Event Reporting to IRBs — Improving Human Subject Protection Jan-2009 III A. ; IV. +

11:50:28, 16 July 2026  +

USA FDA Guidance for Clinical Investigators, Sponsors, and IRBs Adverse Event Reporting to IRBs — Improving Human Subject Protection Jan-2009 Introduction ; III. B. ; Evaluation +

11:50:31, 16 July 2026  +

USA FDA Guidance for Clinical Investigators, Sponsors, and IRBs Adverse Event Reporting to IRBs — Improving Human Subject Protection Jan-2009 Introduction ; III. B. ; IV. +

11:50:29, 16 July 2026  +

USA FDA Guidance for Industry - Computerized Systems Used in Clinical Investigations May-2007 +

12:15:27, 16 July 2026  +