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Property:RefScope
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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 21 CFR Part 312 09-Apr-2025 § 312.32 - Suspected adverse reaction
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GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 2 unexpected adverse reaction
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GBR Directive 2001/20/EC 04-Apr-2001 Article 2 (p)
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USA 21 CFR Part 312 09-Apr-2025 § 312.32 - Unexpected adverse event
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WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 4.10
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WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 7.1 - Investigator
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WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 7.2 - Investigator
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EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 41-001
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DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 40d-002
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GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 32
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GBR Directive 2001/20/EC 04-Apr-2001 Article 16
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USA 21 CFR Part 312 09-Apr-2025 § 312.64 (b)
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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 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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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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