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

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AUT BASG - FAQ 11-Feb-2025 Schwarz +

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USA FDA Guidance for Industry - Electronic Source Data in Clinical Investigations Sep-2013 III 2. +

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USA FDA Guidance for Industry - Computerized Systems Used in Clinical Trials 13-Apr-2015 III +

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USA FDA Guidance for Industry - Computerized Systems Used in Clinical Investigations May-2007 IV +

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USA NIH - SCORE Manual: Appendix Source Documents Requirements Rev 01 16-Aug-2025 Page 3 - CRF +

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USA NIH - SCORE Manual: Appendix Source Documents Requirements Rev 01 16-Aug-2025 Page 3 - Note +

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USA FDA - HUMAN DRUG CGMP NOTES Volume 8, Number 3 6 +

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ICH ICH E6 Guideline R3 (2025) III. Annex 1 4 +

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ICH ICH E6 Guideline R3 (2025) III. Annex 1 2.12.10 +

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ICH ICH E6 Guideline R3 (2025) III. Annex 1 3.16.1 For systems used or deployed by the investigator/institution +

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ICH ICH E6 Guideline R3 (2025) III. Annex 1 4.3 +

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ICH ICH E6 Guideline R3 (2025) III. Annex 1 4.3.3 +

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ICH ICH E6 Guideline R3 (2025) GLOSSARY - Computerised Systems Validation +

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ICH ICH E6 Guideline R3 (2025) III. Annex 1 4.3.4 +

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ICH ICH E6 Guideline R3 (2025) III. Annex 1 4.3.8 +

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

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WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 8 - Electronic data handling +

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EU EMA/INS/GCP/112288/2023 - Guideline on computerised systems and electronic data in clinical trials 2023 4.2 +

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EU EMA/INS/GCP/112288/2023 - Guideline on computerised systems and electronic data in clinical trials 2023 4.4 +

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