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List of results
- Document:AUT MPG – Medizinproduktegesetz 26-May-2022 +
- Document:DEU MPAMIV - Medizinprodukte-Anwendermelde- und Informationsverordnung 21-Apr-2021 +
- Document:DEU MPBetreibV - Medizinprodukte-Betreiberverordnung 24-Apr-2021 +
- Document:EU MDCG Guidelines - +
- Document:EU Regulation (EU) 2017/745 - Medical Device Regulation 05-May-2017 Preamble +
- Document:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 +
- Document:EU ; GBR MDCG 2020-10/1 - Safety reporting in clinical investigations of medical devices 2020 +
- Document:FRA AEC DOC012 v03 Avis aux promoteurs d’investigations cliniques de DM (RIPH1) – Partie II 16-May-2025 +
- Document:FRA AEC-DM-DMDIV DOC006 v04 AAP RDM Partie II Modalités pratiques 16-May-2025 +
- Document:FRA SI RIPH 2G - Website 16-May-2025 +
- Document:GBR Clinical investigations of medical devices – compiling a submission to MHRA May 2021 +
- Document:GBR Directive 90/385/EEC 05-Sep-2007 +
- Document:GBR Directive 93/42/EEC 11-Oct-2007 +
- Document:GBR MEDDEV 2.7/3 revision 3 May-2015 +
- Document:GBR The Medical Devices Regulations 2002 11-Feb-2021 +
- Document:USA 21 CFR Part 812 09-Apr-2025 +
- 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 +
- Document:IMDRF IMDRF – Guidelines - +
- Document:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 +