Property:Query string

"Query string" is a predefined property that describes the conditions of the query as a string and is provided by Semantic MediaWiki. This property is pre-deployed (also known as special property) and comes with additional administrative privileges but can be used just like any other user-defined property.

Usage541

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

[[Reference:+]] [[HasDocument::Document:DEU MBO - Berufsordnung der Ã„rzt:innen 11-Jun-2021]]

DEU MPAMIV - Medizinprodukte-Anwendermelde- und Informationsverordnung 21-Apr-2021 +

[[Reference:+]] [[HasDocument::Document:DEU MPAMIV - Medizinprodukte-Anwendermelde- und Informationsverordnung 21-Apr-2021]]

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

[[Reference:+]] [[HasDocument::Document:DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022]]

DEU SGB V - Sozialgesetzbuch Fünftes Buch 20-Dez-1988 +

[[Reference:+]] [[HasDocument::Document:DEU SGB V - Sozialgesetzbuch Fünftes Buch 20-Dez-1988]]

DEU StrlSchG - Strahlenschutzgesetz 03-Jan-2022 +

[[Reference:+]] [[HasDocument::Document:DEU StrlSchG - Strahlenschutzgesetz 03-Jan-2022]]

DEU TAMG - Tierarzneimittelgesetz 14-Mar-2024 +

[[Reference:+]] [[HasDocument::Document:DEU TAMG - Tierarzneimittelgesetz 14-Mar-2024]]

E

EU 2011/C 172/01 - CT-3 11-Jun-2011 +

[[Reference:+]] [[HasDocument::Document:EU 2011/C 172/01 - CT-3 11-Jun-2011]]

EU COMMISSION IMPLEMENTING DECISION (EU) 2022/729 11-May-2022 +

[[Reference:+]] [[HasDocument::Document:EU COMMISSION IMPLEMENTING DECISION (EU) 2022/729 11-May-2022]]

EU Directive 2001/83/EC - Community code relating to medicinal products for human use 20-Jun-12 +

[[Reference:+]] [[HasDocument::Document:EU Directive 2001/83/EC - Community code relating to medicinal products for human use 20-Jun-12]]

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

[[Reference:+]] [[HasDocument::Document:EU EMA/298712/2022 - Complex clinical trials â€“ Questions and answers 23-May-2022]]

EU EMA/431265/2016 Annex I – to guidance for the conduct of good clinical practice inspections – investigator site 06-Sep-2017 +

[[Reference:+]] [[HasDocument::Document:EU EMA/431265/2016 Annex I â€“ to guidance for the conduct of good clinical practice inspections â€“ investigator site 06-Sep-2017]]

EU EMA/698382/2021 - Guideline for the notification of serious breaches of Regulation (EU) No 536/2014 or the clinical trial protocol 2021 +

[[Reference:+]] [[HasDocument::Document:EU EMA/698382/2021 - Guideline for the notification of serious breaches of Regulation (EU) No 536/2014 or the clinical trial protocol 2021]]

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

[[Reference:+]] [[HasDocument::Document:EU EMA/786433/2022 Annex V â€“ to guidance for the conduct of good clinical practice inspections â€“ Phase I units 15-Nov-2022]]

EU EMA/INS/GCP/112288/2023 - Guideline on computerised systems and electronic data in clinical trials 2023 +

[[Reference:+]] [[HasDocument::Document:EU EMA/INS/GCP/112288/2023 - Guideline on computerised systems and electronic data in clinical trials 2023]]

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

[[Reference:+]] [[HasDocument::Document:EU EMA/INS/GCP/126568/2023 - Annual Report of the Good Clinical Practice (GCP) Inspectors' Working Group (IWG) 2022 2023]]

EU EMA/INS/GCP/143492/2022 - ANNEX I TO PROCEDURE FOR CONDUCTING GCP INSPECTIONS REQUESTED BY THE CHMP: INVESTIGATOR SITE 2022 +

[[Reference:+]] [[HasDocument::Document:EU EMA/INS/GCP/143492/2022 - ANNEX I TO PROCEDURE FOR CONDUCTING GCP INSPECTIONS REQUESTED BY THE CHMP: INVESTIGATOR SITE 2022]]

EU EMA/INS/GCP/856758/ 2018 Guideline on the content, management and archiving of the clinical trial master file (paper and/or electronic) 06-Dec-2018 +

[[Reference:+]] [[HasDocument::Document:EU EMA/INS/GCP/856758/ 2018 Guideline on the content, management and archiving of the clinical trial master file (paper and/or electronic) 06-Dec-2018]]

EU EMEA/CHMP/313666/2005 - GUIDELINE ON THE EXPOSURE TO MEDICINAL PRODUCTS DURING PREGNANCY: NEED FOR POST-AUTHORISATION DATA 14-Nov-2005 +

[[Reference:+]] [[HasDocument::Document:EU EMEA/CHMP/313666/2005 - GUIDELINE ON THE EXPOSURE TO MEDICINAL PRODUCTS DURING PREGNANCY: NEED FOR POST-AUTHORISATION DATA 14-Nov-2005]]

EU ENCePP - Guide on Methodological Standards in Pharmacoepidemiology Revision 11 (2023) +

[[Reference:+]] [[HasDocument::Document:EU ENCePP - Guide on Methodological Standards in Pharmacoepidemiology Revision 11 (2023)]]

EU Eudralex - volume 4 GMP Guidelines Annex 11 Jan-2011 +

[[Reference:+]] [[HasDocument::Document:EU Eudralex - volume 4 GMP Guidelines Annex 11 Jan-2011]]