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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 FD&C Act - Federal Food, Drug, and Cosmetic Act 30-Sep-2023 Sec 510 (k)
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USA FD&C Act - Federal Food, Drug, and Cosmetic Act 30-Sep-2023 Sec 512 (f)
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EN
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USA FD&C Act - Federal Food, Drug, and Cosmetic Act 30-Sep-2023 Sec 737 (8)
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EN
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EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 51
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EN
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EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Annex VIII
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EN
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EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 47
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EN
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EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Annex VIII
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EN
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GBR Directive 93/42/EEC 11-Oct-2007 Article 9
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USA FD&C Act - Federal Food, Drug, and Cosmetic Act 30-Sep-2023 Section 513
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ICH ICH E8 Guideline R1 (2021) ANNEX: TYPES OF CLINICAL STUDIES
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EN
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WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - clinical trial Phases
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EN
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USA 21 CFR Part 312 09-Apr-2025 § 312.21
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EN
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USA 21 CFR Part 312 09-Apr-2025 § 312.85
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EN
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ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 Annex I
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EN
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ICH ICH E6 Guideline - Annex 2 R3 Annex 2 Annex 2 3
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EN
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ICH ICH E8 Guideline R1 (2021) -
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EN
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ICH ICH E8 Guideline R1 (2021) 3.3.5
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EN
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ICH ICH E9 Guideline 1998 III
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EN
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WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 9.1
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EN
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WHO WHO - HANDBOOK FOR GOOD CLINICAL RESEARCH PRACTICE (GCP) 2005 Overview of the Clinical Research Process
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