Property:RefScope

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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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USA 21 CFR Part 812 09-Apr-2025 § 812.150 (a) (1) +

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ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 9.2.5 +

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EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 77 Paragraph 1, 3 & 4 +

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EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 80 Paragraph 1-2 +

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EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 80 Paragraph 3 +

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EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 80 Paragraph 4 +

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EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 80 Paragraph 5 – 6 +

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EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 87 Paragraph 1 – 2 +

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EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 87 Paragraph 3 – 5 +

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EU ; GBR MDCG 2020-10/1 - Safety reporting in clinical investigations of medical devices 2020 8-001 +

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DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 63 +

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DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 64 +

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AUT MPG – Medizinproduktegesetz 26-May-2022 § 22 +

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FRA AEC DOC012 v03 Avis aux promoteurs d’investigations cliniques de DM (RIPH1) – Partie II 16-May-2025 3. +

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FRA AEC DOC012 v03 Avis aux promoteurs d’investigations cliniques de DM (RIPH1) – Partie II 16-May-2025 2.-001 +

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GBR Directive 93/42/EEC 11-Oct-2007 Annex X +

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GBR Clinical investigations of medical devices – compiling a submission to MHRA May 2021 2.-002 +

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EU ; GBR MDCG 2020-10/1 - Safety reporting in clinical investigations of medical devices 2020 8-002 +

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GBR MEDDEV 2.7/3 revision 3 May-2015 4 +

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GBR MEDDEV 2.7/3 revision 3 May-2015 5 - 6 +

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