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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:GBR Data Protection Act 2018 06-Jun-2022  + (06-Jun-2022)
• Document:USA 21 CFR Part 809 06-May-2024  + (06-May-2024)
• Document:EU EMA/431265/2016 Annex I – to guidance for the conduct of good clinical practice inspections – investigator site 06-Sep-2017  + (06-Sep-2017)
• Document:GBR NHS: Records Management Code of Practice 07-Aug-2023  + (07-Aug-2023)
• Document:FRA Guide de légistique 07-Feb-2024  + (07-Feb-2024)
• Document:GBR GUIDANCE FOR THE NOTIFICATION OF SERIOUS BREACHES OF GCP OR THE TRIAL PROTOCOL 08-Jul-2020  + (08-Jul-2020)
• Document:AUT Ärztegesetz 08-Mar-2023  + (08-Mar-2023)
• Document:DEU StrlSchV - Strahlenschutzverordnung 08-Oct-2021  + (08-Oct-2021)
• Document:USA 21 CFR Part 11 09-Apr-2025  + (09-Apr-2025)
• Document:USA 21 CFR Part 312 09-Apr-2025  + (09-Apr-2025)
• Document:USA 21 CFR Part 314 09-Apr-2025  + (09-Apr-2025)
• Document:USA 21 CFR Part 320 09-Apr-2025  + (09-Apr-2025)
• Document:USA 21 CFR Part 50 09-Apr-2025  + (09-Apr-2025)
• Document:USA 21 CFR Part 54 09-Apr-2025  + (09-Apr-2025)
• Document:USA 21 CFR Part 56 09-Apr-2025  + (09-Apr-2025)
• Document:USA 21 CFR Part 812 09-Apr-2025  + (09-Apr-2025)
• Document:USA 42 CFR Part 11 09-Apr-2025  + (09-Apr-2025)
• Document:USA 45 CFR Part 160 09-Apr-2025  + (09-Apr-2025)
• Document:USA 45 CFR Part 46 09-Apr-2025  + (09-Apr-2025)
• Document:DEU AMWHV – Arzneimittel- und Wirkstoffherstellungs-verordnung 09-Aug-2019  + (09-Aug-2019)
• Document:FRA Constitution du 4 octobre 1958 10-Mar-2024  + (10-Mar-2024)
• Document:WHO WHO - ICD 11  + (11)

• Document:GBR The Medical Devices Regulations 2002 11-Feb-2021  + (11-Feb-2021)

• Document:AUT BASG - FAQ 11-Feb-2025  + (11-Feb-2025)
• Document:AUT Question - BASG 11-Feb-2025  + (11-Feb-2025)
• Document:EU 2011/C 172/01 - CT-3 11-Jun-2011  + (11-Jun-2011)
• Document:DEU MBO - Berufsordnung der Ärzt:innen 11-Jun-2021  + (11-Jun-2021)
• Document:EU COMMISSION IMPLEMENTING DECISION (EU) 2022/729 11-May-2022  + (11-May-2022)
• Document:GBR Directive 93/42/EEC 11-Oct-2007  + (11-Oct-2007)
• Document:GBR Making changes to a research study to manage the impact of COVID-19 12-Oct-2021  + (12-Oct-2021)
• Document:USA FDA Guidance for Industry - Computerized Systems Used in Clinical Trials 13-Apr-2015  + (13-Apr-2015)
• Document:FRA DHOS/E1/DAF/DPACI no 2007-322 14-Aug-2007  + (14-Aug-2007)
• Document:DEU TAMG - Tierarzneimittelgesetz 14-Mar-2024  + (14-Mar-2024)
• Document:EU EMEA/CHMP/313666/2005 - GUIDELINE ON THE EXPOSURE TO MEDICINAL PRODUCTS DURING PREGNANCY: NEED FOR POST-AUTHORISATION DATA 14-Nov-2005  + (14-Nov-2005)
• Document:DEU Gemeinsame Empfehlungen - zur Anzeige von Anwendungsbeobachtungen und nichtinterventionellen Unbedenklichkeits-studien 15-Dec-2022  + (15-Dec-2022)
• Document:AUT FAQ - COVID-19 Studien 15-Mar-2021  + (15-Mar-2021)
• Document:EU EMA/786433/2022 Annex V – to guidance for the conduct of good clinical practice inspections – Phase I units 15-Nov-2022  + (15-Nov-2022)
• Document:FRA Bonnes pratiques - CONTRÔLE QUALITÉ À DISTANCE DES ESSAIS CLINIQUES (CNIL) 16-May-2024  + (16-May-2024)
• Document:FRA AEC DOC012 v03 Avis aux promoteurs d’investigations cliniques de DM (RIPH1) – Partie II 16-May-2025  + (16-May-2025)
• Document:FRA AEC-DM-DMDIV DOC006 v04 AAP RDM Partie II Modalités pratiques 16-May-2025  + (16-May-2025)
• Document:FRA Code de la Santé Publique - Partie législative - 1ere partie, Livre 1er, Titre II 16-May-2025  + (16-May-2025)
• Document:FRA Code de la Santé Publique - Partie Réglementaire - 1ere partie, Livre 1er, Titre II 16-May-2025  + (16-May-2025)
• Document:FRA SI RIPH 2G - Website 16-May-2025  + (16-May-2025)
• Document:FRA SURV VIG DOC118 V01 REC-Avis aux promoteurs -Partie V 16-May-2025  + (16-May-2025)
• Document:GBR Guidance Managing clinical trials during Coronavirus (COVID-19) 16-Nov-.2021  + (16-Nov-.2021)
• Document:GBR Guidance - Good clinical practice for clinical trials 16-Oct-2015  + (16-Oct-2015)
• Document:EU Regulation (EU) 910/2014 - electronic identification 17-Sep-2014  + (17-Sep-2014)
• Document:DEU AMG - Arzneimittelgesetz 19-Jul-2023  + (19-Jul-2023)