Property:RefModule

Module number this reference belongs to.

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.

I

IMDRF IMDRF – Guidelines - - +

4 +

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

4 +

ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 7.11 +

4 +

E

EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 ANNEX I Section D No. 17 +

4 +

EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 2 +

4 +

EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 109 Paragraph 1-001 +

4 +

I

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

4 +

W

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

4 +

WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 4.12-003 +

4 +

WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 11.2 +

4 +

E

EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 78 +

4 +

EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 72 Pragraph 5 +

4 +

EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 109 Paragraph 1-002 +

4 +

EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 68 Paragraph 5 +

4 +

EU INS/GCP/46309/2012 - Classification and analysis of the GCP inspection findings of GCP inspections conducted at the request of the CHMP 2012 5 +

4 +

EU EMA/INS/GCP/126568/2023 - Annual Report of the Good Clinical Practice (GCP) Inspectors' Working Group (IWG) 2022 2023 3.1.2 a) +

4 +

EU EMA/INS/GCP/126568/2023 - Annual Report of the Good Clinical Practice (GCP) Inspectors' Working Group (IWG) 2022 2023 4.3 +

4 +

EU EMA/786433/2022 Annex V – to guidance for the conduct of good clinical practice inspections – Phase I units 15-Nov-2022 2.5-002 +

4 +

D

DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 42c +

4 +

DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 68 +

4 +

Personal tools

Search

About the Database

Navigation

Structure

Tools

Property:RefModule

From GxPlex

	This page was last edited on 12 October 2026, at 03:24. Content is available under Creative Commons Attribution unless otherwise noted. Datenschutzrichtlinie Impressum
	Mozilla Cavendish skin Report a bug – Skin version: 3.0.0