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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:USA 21 CFR Part 50 09-Apr-2025  + (21 CFR Part 50)

• Document:USA 21 CFR Part 54 09-Apr-2025  + (21 CFR Part 54)
• Document:USA 21 CFR Part 56 09-Apr-2025  + (21 CFR Part 56)
• Document:USA 21 CFR Part 809 06-May-2024  + (21 CFR Part 809)
• Document:USA 21 CFR Part 812 09-Apr-2025  + (21 CFR Part 812)
• Document:USA 42 CFR Part 11 09-Apr-2025  + (42 CFR Part 11)
• Document:USA 45 CFR Part 160 09-Apr-2025  + (45 CFR Part 160)
• Document:USA 45 CFR Part 46 09-Apr-2025  + (45 CFR Part 46)
• Document:FRA AEC-DM-DMDIV DOC006 v04 AAP RDM Partie II Modalités pratiques 16-May-2025  + (AEC-DM-DMDIV_DOC006 v04 AAP_RDM_Partie II_Modalités pratiques)
• Document:FRA AEC DOC010 V.04 01-Jun-2018  + (AEC_DOC010 V.04)
• Document:FRA AEC DOC012 v03 Avis aux promoteurs d’investigations cliniques de DM (RIPH1) – Partie II 16-May-2025  + (AEC_DOC012 v03 Avis aux promoteurs d’investigations cliniques de DM (RIPH1) – Partie II)
• Document:DEU AMG - Arzneimittelgesetz 19-Jul-2023  + (AMG - Arzneimittelgesetz)
• Document:AUT AMG – Arzneimittelgesetz 04-Mar-2023  + (AMG – Arzneimittelgesetz)
• Document:DEU AMWHV – Arzneimittel- und Wirkstoffherstellungs-verordnung 09-Aug-2019  + (AMWHV – Arzneimittel- und Wirkstoffherstellungs-verordnung)
• Document:AUT AVG – Allgemeines Verwaltungsverfahrens-gesetz 23-Nov-2021  + (AVG – Allgemeines Verwaltungsverfahrens-gesetz)
• Document:USA Acceptance of Clinical Data to Support Medical Device Applications and Submissions Frequently Asked Questions - Guidance for Industry and Food and Drug Administration Staff 21-Feb-2018  + (Acceptance of Clinical Data to Support Medical Device Applications and Submissions Frequently Asked Questions - Guidance for Industry and Food and Drug Administration Staff)
• Document:N.A. Article from Mora et al. 2023  + (Article from Mora et al.)
• Document:AUT BASG - FAQ 11-Feb-2025  + (BASG - FAQ)
• Document:DEU BGB - Bürgerliches Gesetzbuch 22-Dec-2023  + (BGB - Bürgerliches Gesetzbuch)
• Document:FRA Bonnes pratiques - CONTRÔLE QUALITÉ À DISTANCE DES ESSAIS CLINIQUES (CNIL) 16-May-2024  + (Bonnes pratiques - CONTRÔLE QUALITÉ À DISTANCE DES ESSAIS CLINIQUES (CNIL))
• Document:DEU Bundestag - Sachstand zur Aufbewahrung von Patientenakten in der ambulanten Praxis Fristen und Form 01-Mar-2021  + (Bundestag - Sachstand zur Aufbewahrung von Patientenakten in der ambulanten Praxis Fristen und Form)
• Document:EU CHMP Guidelines -  + (CHMP Guidelines)
• Document:CIOMS CIOMS - International Ethical Guidelines for Health-related Research Involving Humans 2016  + (CIOMS - International Ethical Guidelines for Health-related Research Involving Humans)
• Document:CIOMS CIOMS - International Ethical Guidelines for Biomedical Research Involving Human Subjects 2016  + (CIOMS - International Ethical Guidelines for Biomedical Research Involving Human Subjects)
• Document:CIOMS CIOMS Publications -  + (CIOMS Publications)
• Document:EU COMMISSION IMPLEMENTING DECISION (EU) 2022/729 11-May-2022  + (COMMISSION IMPLEMENTING DECISION (EU) 2022/729)
• Document:USA CTCAE - Common Terminology Criteria for Adverse Events v5.0 (2017)  + (CTCAE - Common Terminology Criteria for Adverse Events)
• Document:GBR Clinical Trial toolkit 28-Jan-2025  + (Clinical Trial toolkit)
• Document:GBR Clinical investigations of medical devices – compiling a submission to MHRA May 2021  + (Clinical investigations of medical devices – compiling a submission to MHRA)
• Document:FRA Code de la Santé Publique - Partie Réglementaire - 1ere partie, Livre 1er, Titre II 16-May-2025  + (Code de la Santé Publique - Partie Réglementaire - 1ere partie, Livre 1er, Titre II)
• Document:FRA Code de la Santé Publique - Partie législative - 1ere partie, Livre 1er, Titre II 16-May-2025  + (Code de la Santé Publique - Partie législative - 1ere partie, Livre 1er, Titre II)
• Document:FRA Constitution du 4 octobre 1958 10-Mar-2024  + (Constitution du 4 octobre 1958)
• Document:DEU DGEPi - GEP Guter Epidemiologischer Praxis Sep-2018  + (DGEPi - GEP Guter Epidemiologischer Praxis)
• Document:FRA DHOS/E1/DAF/DPACI no 2007-322 14-Aug-2007  + (DHOS/E1/DAF/DPACI no 2007-322)
• Document:GBR Data Protection Act 2018 06-Jun-2022  + (Data Protection Act 2018)
• Document:WMA Declaration of Helsinki 2024  + (Declaration of Helsinki)
• Document:DEU Deutsches Ärzteblatt 45849  + (Deutsches Ärzteblatt)
• Document:GBR Directive 2001/20/EC 04-Apr-2001  + (Directive 2001/20/EC)
• Document:EU Directive 2001/83/EC - Community code relating to medicinal products for human use 20-Jun-12  + (Directive 2001/83/EC - Community code relating to medicinal products for human use)
• Document:GBR Directive 90/385/EEC 05-Sep-2007  + (Directive 90/385/EEC)
• Document:GBR Directive 93/42/EEC 11-Oct-2007  + (Directive 93/42/EEC)
• Document:GBR Directive 98/79/EC 20-Dec-2011  + (Directive 98/79/EC)
• Document:EU EMA Guidelines -  + (EMA Guidelines)
• Document:EU EMA/298712/2022 - Complex clinical trials – Questions and answers 23-May-2022  + (EMA/298712/2022 - Complex clinical trials – Questions and answers)