Property:DocVersion

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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.

A

AUT AVG – Allgemeines Verwaltungsverfahrens-gesetz 23-Nov-2021 +

23-Nov-2021 +

D

DEU MPBetreibV - Medizinprodukte-Betreiberverordnung 24-Apr-2021 +

24-Apr-2021 +

E

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

25-Apr-2017 +

A

AUT MPG – Medizinproduktegesetz 26-May-2022 +

26-May-2022 +

E

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

27-May-2014 Preamble +

U

USA NIH - Glossary 27-May-2025 +

27-May-2025 +

G

GBR Clinical Trial toolkit 28-Jan-2025 +

28-Jan-2025 +

GBR HRA - Ending your project 28-Jan-2025 +

28-Jan-2025 +

GBR IRAS - Integrated Research Application System 28-Jan-2025 +

28-Jan-2025 +

GBR NIHR - National Institute for Health and Care Research 28-Jan-2025 +

28-Jan-2025 +

E

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

28-Jan-22 +

D

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

28-Jun-2022 +

A

AUT LekV – Leit-Ethikkommissions-Verordnung 29-Nov-2024 +

29-Nov-2024 +

U

USA NCI GUIDELINES FOR INVESTIGATORS: ADVERSE EVENT REPORTING REQUIREMENTS FOR DCTD (CTEP AND CIP) INDs AND IDEs 30-Aug-2024 +

30-Aug-2024 +

USA FD&C Act - Federal Food, Drug, and Cosmetic Act 30-Sep-2023 +

30-Sep-2023 +

USA U.S. Code Title 21 30-Sep-2023 +

30-Sep-2023 +

G

GBR UK GDPR - United Kingdom General Data Protection Regulation 31-Dec-2020 +

31-Dec-2020 +

D

DEU KPBV - Klinische Prüfung-Bewertungsverfahren-Verordnung 31-Jan-2022 +

31-Jan-2022 +

N

N.A. (STROBE)statement: guidelines for reporting observational studies Apr-2008 +

Apr-2008 +

U

USA FDA Guidance for Industry - Oversight of Clinical Investigations — A Risk-Based Approach to Monitoring Aug-2013 +

Aug-2013 +

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	This page was last edited on 6 October 2026, at 20:03. Content is available under Creative Commons Attribution unless otherwise noted. Datenschutzrichtlinie Impressum
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