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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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EU Recommendations of the expert group - Risk proportionate approaches in clinical trials 25-Apr-2017 2. +

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EU Recommendations of the expert group - Risk proportionate approaches in clinical trials 25-Apr-2017 4.1 +

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EU EMA/298712/2022 - Complex clinical trials – Questions and answers 23-May-2022 - +

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EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 62 Paragraph 1 +

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EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 62 Paragraph 3 +

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EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 74 +

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EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 82 +

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EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 58 Paragraph 1 – 3 +

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EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 58 Paragraph 5-001 +

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EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 70 +

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DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 3 Absatz 4 +

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DEU DGEPi - GEP Guter Epidemiologischer Praxis Sep-2018 Leitlinie 2 +

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DEU DGEPi - GEP Guter Epidemiologischer Praxis Sep-2018 Leitlinie 3 3.3 - 3.6 +

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DEU DGEPi - GEP Guter Epidemiologischer Praxis Sep-2018 Leitlinie 6 6.1 +

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USA 21 CFR Part 312 09-Apr-2025 § 312.23 (6) (d) +

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USA 21 CFR Part 314 09-Apr-2025 § 314.126 +

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ICH ICH E9 Guideline - Addendum R1 20-Nov-2019 - +

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WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 9.3 +

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ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 Annex A A.7 +

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EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Annex XV Chapter I Section 2 +

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