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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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WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 4.6
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ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 Annex A A.6.3-002
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GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 30-001
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GBR Directive 2001/20/EC 04-Apr-2001 Article 10 (b)-001
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USA 21 CFR Part 312 09-Apr-2025 § 312.30 (b) (ii)
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USA 21 CFR Part 812 09-Apr-2025 § 812.150 (a) (4)
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ICH ICH E6 Guideline R3 (2025) Appendix B 4.8-002
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ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 3.46
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ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 7.4.3-002
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EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 54
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EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 77
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EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 72 Paragraph 6
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EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 76
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EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 77
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EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 68 Paragraph 1
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USA 21 CFR Part 812 09-Apr-2025 § 812.46 (b)
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GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 30-002
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GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 31
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GBR Directive 2001/20/EC 04-Apr-2001 Article 10 (b)-002
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GBR Directive 93/42/EEC 11-Oct-2007 Article 15 6. - 7.-001
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