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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.

E

EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 58 Paragraph 7 – 8 +

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

EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Annex XIV Chapter II Section 1.12 +

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

D

DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 40d-001 +

DEU AMG - Arzneimittelgesetz 19-Jul-2023 +

DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 3 Absatz 5 – 6 +

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

DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 30-002 +

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

DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 62-001 +

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

DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 65 +

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

U

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

USA 21 CFR Part 312 09-Apr-2025 +

USA FDA Guidance for Industry Investigator Responsibilities — Protecting the Rights, Safety, and Welfare of Study Subjects Oct-2009 III. A. +

USA FDA Guidance for Industry Investigator Responsibilities — Protecting the Rights, Safety, and Welfare of Study Subjects Oct-2009 +

I

ICH ICH E6 Guideline R3 (2025) III. Annex 1 2.2 +

ICH ICH E6 Guideline R3 (2025) +

W

WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 4.7 +

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

I

ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 10.3 +

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

E

EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 50 +

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

D

DEU DGEPi - GEP Guter Epidemiologischer Praxis Sep-2018 Leitlinie 3 3.9 +

DEU DGEPi - GEP Guter Epidemiologischer Praxis Sep-2018 +

DEU DGEPi - GEP Guter Epidemiologischer Praxis Sep-2018 Leitlinie 6 6.4 +

DEU DGEPi - GEP Guter Epidemiologischer Praxis Sep-2018 +

G

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

GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 +

GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Schedule 3 Part 1 1. +

GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 +

I

ICH ICH E6 Guideline R3 (2025) III. Annex 1 3.5 +

ICH ICH E6 Guideline R3 (2025) +

ICH ICH E6 Guideline R3 (2025) GLOSSARY - Agreement +

ICH ICH E6 Guideline R3 (2025) +

ICH ICH E6 Guideline R3 (2025) III. Annex 1 3.6 +

ICH ICH E6 Guideline R3 (2025) +

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	This page was last edited on 9 October 2026, at 06:03. Content is available under Creative Commons Attribution unless otherwise noted. Datenschutzrichtlinie Impressum
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