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

previous 202050100250500next 20

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 Eudralex - volume 4 GMP Guidelines Chapter 4 Jan-2011 +

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

EU GUIDANCE ON THE MANAGEMENT OF CLINICAL TRIALS DURING THE COVID-19 (CORONAVIRUS) PANDEMIC v5 10-Feb-2022 +

[[Reference:+]] [[HasDocument::Document:EU GUIDANCE ON THE MANAGEMENT OF CLINICAL TRIALS DURING THE COVID-19 (CORONAVIRUS) PANDEMIC v5 10-Feb-2022]]

EU GVP: Module VIII EMA/813938/2011 Rev. 3 (2017) +

[[Reference:+]] [[HasDocument::Document:EU GVP: Module VIII EMA/813938/2011 Rev. 3 (2017)]]

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

[[Reference:+]] [[HasDocument::Document:EU INS/GCP/46309/2012 - Classification and analysis of the GCP inspection findings of GCP inspections conducted at the request of the CHMP 2012]]

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

[[Reference:+]] [[HasDocument::Document:EU Recommendations of the expert group - Risk proportionate approaches in clinical trials 25-Apr-2017]]

EU Regulation (EC) No 726/2004 - authorisation and supervision of medicinal products for human use 28-Jan-22 +

[[Reference:+]] [[HasDocument::Document:EU Regulation (EC) No 726/2004 - authorisation and supervision of medicinal products for human use 28-Jan-22]]

EU Regulation (EU) 2016/679 (GDPR) 04-May-2016 +

[[Reference:+]] [[HasDocument::Document:EU Regulation (EU) 2016/679 (GDPR) 04-May-2016]]

EU Regulation (EU) 2017/745 - Medical Device Regulation 05-May-2017 Preamble +

[[Reference:+]] [[HasDocument::Document:EU Regulation (EU) 2017/745 - Medical Device Regulation 05-May-2017 Preamble]]

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

[[Reference:+]] [[HasDocument::Document:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023]]

EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 05-May-2017 Preamble +

[[Reference:+]] [[HasDocument::Document:EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 05-May-2017 Preamble]]

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

[[Reference:+]] [[HasDocument::Document:EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023]]

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

[[Reference:+]] [[HasDocument::Document:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022]]

EU Regulation (EU) 536/2014 - clinical trials 27-May-2014 Preamble +

[[Reference:+]] [[HasDocument::Document:EU Regulation (EU) 536/2014 - clinical trials 27-May-2014 Preamble]]

EU Regulation (EU) 910/2014 - electronic identification 17-Sep-2014 +

[[Reference:+]] [[HasDocument::Document:EU Regulation (EU) 910/2014 - electronic identification 17-Sep-2014]]

EU Regulation (EU) No 520/2012 - performance of pharmacovigilance activities 20-Jun-12 +

[[Reference:+]] [[HasDocument::Document:EU Regulation (EU) No 520/2012 - performance of pharmacovigilance activities 20-Jun-12]]

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

[[Reference:+]] [[HasDocument::Document:EU ; GBR MDCG 2020-10/1 - Safety reporting in clinical investigations of medical devices 2020]]

EU ; GBR Regulation (EC) No 1223/2009 - Cosmetic Products 01-Dec-2023 +

[[Reference:+]] [[HasDocument::Document:EU ; GBR Regulation (EC) No 1223/2009 - Cosmetic Products 01-Dec-2023]]

EU ; GBR Regulation (EC) No 178/2002 - Food Safety 01-Jul-2022 +

[[Reference:+]] [[HasDocument::Document:EU ; GBR Regulation (EC) No 178/2002 - Food Safety 01-Jul-2022]]

EUR European Bioethics Convention 1997 +

[[Reference:+]] [[HasDocument::Document:EUR European Bioethics Convention 1997]]

F

FRA AEC DOC010 V.04 01-Jun-2018 +

[[Reference:+]] [[HasDocument::Document:FRA AEC DOC010 V.04 01-Jun-2018]]