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This page provides a simple browsing interface for finding entities described by a property and a named value. Other available search interfaces include the page property search, and the ask query builder.

List of results

• Document:EU CHMP Guidelines -  + (Corpus of texts)
• Document:EU EMA Guidelines -  + (Corpus of texts)
• Document:EU EudraLex – Volume 10 -  + (Corpus of texts)
• Document:EU Eudralex - volume 4 GMP Guidelines Annex 11 Jan-2011  + (Corpus of texts)
• Document:EU Eudralex - volume 4 GMP Guidelines Chapter 4 Jan-2011  + (Corpus of texts)
• Document:EU MDCG Guidelines -  + (Corpus of texts)
• Document:USA NIH - SCORE Manual N.A.  + (Corpus of texts)
• Document:USA Recognized Consensus Standards N.A.  + (Corpus of texts)
• Document:CIOMS CIOMS Publications -  + (Corpus of texts)
• Document:ICH ICH Guidelines -  + (Corpus of texts)
• Document:IMDRF IMDRF – Guidelines -  + (Corpus of texts)
• Document:WHO World Health Organization -  + (Corpus of texts)

• Document:AUT BASG - FAQ 11-Feb-2025  + (Information from official body)
• Document:AUT FAQ - COVID-19 Studien 15-Mar-2021  + (Information from official body)
• Document:EU EMA/298712/2022 - Complex clinical trials – Questions and answers 23-May-2022  + (Information from official body)
• 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  + (Information from official body)
• Document:FRA Guide de légistique 07-Feb-2024  + (Information from official body)
• Document:FRA Infographie - La hiérarchie des normes 22-Mar-2024  + (Information from official body)
• Document:FRA SI RIPH 2G - Website 16-May-2025  + (Information from official body)
• Document:GBR Clinical Trial toolkit 28-Jan-2025  + (Information from official body)
• Document:GBR IRAS - Integrated Research Application System 28-Jan-2025  + (Information from official body)
• Document:GBR NIHR - National Institute for Health and Care Research 28-Jan-2025  + (Information from official body)
• Document:USA NIH - Glossary 27-May-2025  + (Information from official body)
• Document:USA FDA Information - Observations and citations 20-Mar-2024  + (Information from official body)
• Document:DEU Deutsches Ärzteblatt 45849  + (Information from official body)
• Document:EU European Medicines Agency’s Data Protection: Notice For Microsoft (MS) Copilot 365 - EMA pilot phase ; EMA/216030/2025 45838  + (Information from official body)
• Document:GBR MHRA GCP Inspection Dossier template V7.0  + (Information from official body)
• Document:USA WARNING LETTER - Purolea Cosmetics Lab MARCS-CMS 722591 46114  + (Information from official body)
• Document:DEU Richtlinie zur Bewertung der Qualifikation von Prüfern, Hauptprüfern, Leitern und ärztlichen Mitgliedern von Prüfungsteams durch Ethik-Kommissionen von Arbeitskreis Medizinischer Ethik-Kommissionen in der Bundesrepublik Deutschland e. V. und  + (Information from official body)
• Document:CIOMS CIOMS - International Ethical Guidelines for Biomedical Research Involving Human Subjects 2016  + (International guideline)
• Document:CIOMS CIOMS - International Ethical Guidelines for Health-related Research Involving Humans 2016  + (International guideline)
• Document:ICH ICH E11 Guideline R1 (2017)  + (International guideline)
• Document:ICH ICH E19 Guideline 2022  + (International guideline)
• Document:ICH ICH E21 Concept paper 2023  + (International guideline)
• Document:ICH ICH E2A Guideline 1994  + (International guideline)
• Document:ICH ICH E2F Guideline 2010  + (International guideline)
• Document:ICH ICH E3 Guideline 1995  + (International guideline)
• Document:ICH ICH E6 Guideline R3 (2025)  + (International guideline)
• Document:ICH ICH E6 Guideline - Annex 2 R3 Annex 2  + (International guideline)
• Document:ICH ICH E7 Guideline 1993  + (International guideline)
• Document:ICH ICH E8 Guideline R1 (2021)  + (International guideline)
• Document:ICH ICH E9 Guideline - Addendum R1 20-Nov-2019  + (International guideline)
• Document:ICH ICH E9 Guideline 1998  + (International guideline)
• Document:INT ISPE - GPP Revision 3 (2015)  + (International guideline)
• Document:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020  + (International guideline)
• Document:N.A. (STROBE)statement: guidelines for reporting observational studies Apr-2008  + (International guideline)
• Document:WHO WHO - Guidance for best practices for clinical trials 2024  + (International guideline)
• Document:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995  + (International guideline)
• Document:WHO WHO - HANDBOOK FOR GOOD CLINICAL RESEARCH PRACTICE (GCP) 2005  + (International guideline)
• Document:WHO WHO - ICD 11  + (International guideline)