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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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ICH ICH E6 Guideline R3 (2025) III. Annex 1 3.14-001 +

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WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - contract +

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WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 4.11 +

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ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 6.9 +

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DEU MBO - Berufsordnung der Ärzt:innen 11-Jun-2021 § 33 +

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DEU Gemeinsame Empfehlungen - zur Anzeige von Anwendungsbeobachtungen und nichtinterventionellen Unbedenklichkeits-studien 15-Dec-2022 2.7.7 +

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DEU DGEPi - GEP Guter Epidemiologischer Praxis Sep-2018 Leitlinie 9 +

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FRA Code de la Santé Publique - Partie Réglementaire - 1ere partie, Livre 1er, Titre II 16-May-2025 Article R1121-3-1 +

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GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 15 (5) (k)-(l) +

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GBR IRAS - Integrated Research Application System 28-Jan-2025 Templates +

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USA 21 CFR Part 312 09-Apr-2025 § 312.53 (c) +

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USA 21 CFR Part 812 09-Apr-2025 § 812.43 (c) (5) +

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WMA Declaration of Helsinki 2024 Paragraph 9 +

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ICH ICH E6 Guideline R3 (2025) III. Annex 1 2.7.1-001 +

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WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - escape treatment +

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WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 4.1 +

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ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 10.7 +

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EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 28 Paragraph 1 (f) +

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EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 62 Paragraph 4 (j) +

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EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 58 Paragraph 5 (j) +

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