Property:RefModule

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Usage1181

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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ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 3.52 +

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ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 Annex F +

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EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 2 Paragraph 64 – 66 +

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EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 2 Paragraph 67–69 +

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DEU MPAMIV - Medizinprodukte-Anwendermelde- und Informationsverordnung 21-Apr-2021 § 2 +

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ICH ICH E6 Guideline R3 (2025) III. Annex 1 2.7.2 (a) - (d) +

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ICH ICH E6 Guideline - Annex 2 R3 Annex 2 Annex 2 2.4 - 2.5 +

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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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ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 10.8 +

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EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 41-001 +

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EU ; GBR MDCG 2020-10/1 - Safety reporting in clinical investigations of medical devices 2020 8.2-001 +

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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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GBR Clinical investigations of medical devices – compiling a submission to MHRA May 2021 2.-001 +

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EU ; GBR MDCG 2020-10/1 - Safety reporting in clinical investigations of medical devices 2020 8.2-002 +

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GBR MEDDEV 2.7/3 revision 3 May-2015 7.2 +

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USA 21 CFR Part 312 09-Apr-2025 § 312.64 (b) +

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	This page was last edited on 12 October 2026, at 03:24. Content is available under Creative Commons Attribution unless otherwise noted. Datenschutzrichtlinie Impressum
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