Search by property

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:CIOMS CIOMS - International Ethical Guidelines for Health-related Research Involving Humans 2016  + (12:15:29, 16 July 2026)
• Document:ICH ICH E6 Guideline R3 (2025)  + (12:15:29, 16 July 2026)
• Document:ICH ICH E2F Guideline 2010  + (12:15:29, 16 July 2026)
• Document:ICH ICH E2A Guideline 1994  + (12:15:29, 16 July 2026)
• Document:ICH ICH E19 Guideline 2022  + (12:15:29, 16 July 2026)
• Document:ICH ICH E21 Concept paper 2023  + (12:15:29, 16 July 2026)
• Document:CIOMS CIOMS - International Ethical Guidelines for Biomedical Research Involving Human Subjects 2016  + (12:15:29, 16 July 2026)
• Document:ICH ICH E3 Guideline 1995  + (12:15:29, 16 July 2026)
• Document:ICH ICH E8 Guideline R1 (2021)  + (12:15:30, 16 July 2026)
• Document:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020  + (12:15:30, 16 July 2026)
• Document:ICH ICH E9 Guideline 1998  + (12:15:30, 16 July 2026)
• Document:INT Nuremberg Code 1947  + (12:15:30, 16 July 2026)
• Document:IMDRF IMDRF – Guidelines -  + (12:15:30, 16 July 2026)
• Document:ICH ICH E7 Guideline 1993  + (12:15:30, 16 July 2026)
• Document:ICH ICH E9 Guideline - Addendum R1 20-Nov-2019  + (12:15:30, 16 July 2026)
• Document:INT ISPE - GPP Revision 3 (2015)  + (12:15:30, 16 July 2026)
• Document:WHO WHO - EXPERT COMMITTEE ON SPECIFICATIONS FOR PHARMACEUTICAL PREPARATIONS Forty-fifth report  + (12:15:31, 16 July 2026)
• Document:N.A. Article from Mora et al. 2023  + (12:15:31, 16 July 2026)
• Document:WHO WHO - Guidance for best practices for clinical trials 2024  + (12:15:31, 16 July 2026)
• Document:N.A. (STROBE)statement: guidelines for reporting observational studies Apr-2008  + (12:15:31, 16 July 2026)
• Document:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995  + (12:15:31, 16 July 2026)
• Document:N.A. SPIRIT 2013 - Chan et al. 2013  + (12:15:31, 16 July 2026)

• Document:WHO WHO - HANDBOOK FOR GOOD CLINICAL RESEARCH PRACTICE (GCP) 2005  + (12:15:32, 16 July 2026)
• Document:WMA Declaration of Helsinki 2024  + (12:15:32, 16 July 2026)
• Document:DEU Deutsches Ärzteblatt 45849  + (12:15:32, 16 July 2026)
• Document:EU European Medicines Agency’s Data Protection: Notice For Microsoft (MS) Copilot 365 - EMA pilot phase ; EMA/216030/2025 45838  + (12:15:32, 16 July 2026)
• Document:WHO WHO Good Practices for Clinical Trial Design and Implementation 04-May-2026  + (12:15:32, 16 July 2026)
• Document:N.A. Minimum Criteria for ICH E6 (R3) GCP Investigator Site Personnel Training V3.0  + (12:15:32, 16 July 2026)
• Document:N.A. Transcelerate GCP mutual recognition programm FAQ 21-May-2025  + (12:15:32, 16 July 2026)
• Document:GBR MHRA GCP Inspection Dossier template V7.0  + (12:15:32, 16 July 2026)
• Document:USA WARNING LETTER - Purolea Cosmetics Lab MARCS-CMS 722591 46114  + (12:15:32, 16 July 2026)
• 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  + (12:15:32, 16 July 2026)

• Property:RefTags  + (12:18:06, 16 July 2026)
• Property:RefModule  + (12:18:08, 16 July 2026)
• Property:RefUnit  + (12:18:08, 16 July 2026)
• Property:RefPreview  + (12:18:09, 16 July 2026)
• Document:USA 21 CFR Part 312 09-Apr-2025  + (12:46:53, 16 July 2026)
• Contribute to GxPlex  + (16:42:57, 19 July 2026)
• About GxPlex  + (19:20:31, 19 July 2026)
• The Project  + (20:13:54, 19 July 2026)
• How to start  + (20:15:46, 19 July 2026)
• Main Page  + (20:21:31, 19 July 2026)
• GxPlex:About  + (09:42:24, 13 September 2026)
• GxPlex:Privacy policy  + (10:07:25, 13 September 2026)