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Property:RefLanguage
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<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 NCI GUIDELINES FOR INVESTIGATORS: ADVERSE EVENT REPORTING REQUIREMENTS FOR DCTD (CTEP AND CIP) INDs AND IDEs 30-Aug-2024 5.3.2
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ICH ICH E2A Guideline 1994 III B. - III C.
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EN
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ICH ICH E2A Guideline 1994 III E
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EN
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ICH ICH E6 Guideline R3 (2025) III. Annex 1 3.13.2 (a) - (b) ; (d) - (f)
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EN
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WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 5.13
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WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 7.1 - Sponsor
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WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 7.2 - Sponsor
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ICH ICH E6 Guideline R3 (2025) GLOSSARY - Independent Data Monitoring Committee (IDMC)
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ICH ICH E6 Guideline R3 (2025) III. Annex 1 3.9
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ICH ICH E6 Guideline R3 (2025) Appendix B 8
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ICH ICH E9 Guideline 1998 Glossary - IDMC
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WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 7.1 - Committee
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WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 13
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WHO WHO - HANDBOOK FOR GOOD CLINICAL RESEARCH PRACTICE (GCP) 2005 Page 78
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ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 9.2.5
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ICH ICH E2F Guideline 2010 1
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ICH ICH E6 Guideline R3 (2025) III. Annex 1 3.13.2 (c)
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EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 41-002
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EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 42
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EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 43
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