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:EU Regulation (EU) 2016/679 (GDPR) 04-May-2016  + (EU Regulation (EU) 2016/679 (GDPR) 04-May-2016)
• Document:EU Regulation (EU) 2017/745 - Medical Device Regulation 05-May-2017 Preamble  + (EU Regulation (EU) 2017/745 - Medical Device Regulation 05-May-2017 Preamble)
• Document:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023  + (EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023)
• Document:EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023  + (EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023)
• Document:EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 05-May-2017 Preamble  + (EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 05-May-2017 Preamble)
• Document:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022  + (EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022)
• Document:EU Regulation (EU) 536/2014 - clinical trials 27-May-2014 Preamble  + (EU Regulation (EU) 536/2014 - clinical trials 27-May-2014 Preamble)
• Document:EU Regulation (EU) 910/2014 - electronic identification 17-Sep-2014  + (EU Regulation (EU) 910/2014 - electronic identification 17-Sep-2014)
• Document:EU Regulation (EU) No 520/2012 - performance of pharmacovigilance activities 20-Jun-12  + (EU Regulation (EU) No 520/2012 - performance of pharmacovigilance activities 20-Jun-12)
• Document:EU ; GBR MDCG 2020-10/1 - Safety reporting in clinical investigations of medical devices 2020  + (EU ; GBR MDCG 2020-10/1 - Safety reporting in clinical investigations of medical devices 2020)
• Document:EU ; GBR Regulation (EC) No 1223/2009 - Cosmetic Products 01-Dec-2023  + (EU ; GBR Regulation (EC) No 1223/2009 - Cosmetic Products 01-Dec-2023)
• Document:EU ; GBR Regulation (EC) No 178/2002 - Food Safety 01-Jul-2022  + (EU ; GBR Regulation (EC) No 178/2002 - Food Safety 01-Jul-2022)
• Document:EUR European Bioethics Convention 1997  + (EUR European Bioethics Convention 1997)
• Document:FRA AEC-DM-DMDIV DOC006 v04 AAP RDM Partie II Modalités pratiques 16-May-2025  + (FRA AEC-DM-DMDIV_DOC006 v04 AAP_RDM_Partie II_Modalités pratiques 16-May-2025)
• Document:FRA AEC DOC010 V.04 01-Jun-2018  + (FRA AEC_DOC010 V.04 01-Jun-2018)
• Document:FRA AEC DOC012 v03 Avis aux promoteurs d’investigations cliniques de DM (RIPH1) – Partie II 16-May-2025  + (FRA AEC_DOC012 v03 Avis aux promoteurs d’investigations cliniques de DM (RIPH1) – Partie II 16-May-2025)
• Document:FRA Bonnes pratiques - CONTRÔLE QUALITÉ À DISTANCE DES ESSAIS CLINIQUES (CNIL) 16-May-2024  + (FRA Bonnes pratiques - CONTRÔLE QUALITÉ À DISTANCE DES ESSAIS CLINIQUES (CNIL) 16-May-2024)
• Document:FRA Code de la Santé Publique - Partie Réglementaire - 1ere partie, Livre 1er, Titre II 16-May-2025  + (FRA Code de la Santé Publique - Partie Réglementaire - 1ere partie, Livre 1er, Titre II 16-May-2025)
• Document:FRA Code de la Santé Publique - Partie législative - 1ere partie, Livre 1er, Titre II 16-May-2025  + (FRA Code de la Santé Publique - Partie législative - 1ere partie, Livre 1er, Titre II 16-May-2025)
• Document:FRA Constitution du 4 octobre 1958 10-Mar-2024  + (FRA Constitution du 4 octobre 1958 10-Mar-2024)
• Document:FRA DHOS/E1/DAF/DPACI no 2007-322 14-Aug-2007  + (FRA DHOS/E1/DAF/DPACI no 2007-322 14-Aug-2007)
• Document:FRA Guide de légistique 07-Feb-2024  + (FRA Guide de légistique 07-Feb-2024)
• Document:FRA Infographie - La hiérarchie des normes 22-Mar-2024  + (FRA Infographie - La hiérarchie des normes 22-Mar-2024)
• Document:FRA SI RIPH 2G - Website 16-May-2025  + (FRA SI RIPH 2G - Website 16-May-2025)
• Document:FRA SURV VIG DOC118 V01 REC-Avis aux promoteurs -Partie V 16-May-2025  + (FRA SURV_VIG_DOC118 V01 REC-Avis aux promoteurs -Partie V 16-May-2025)

• Document:GBR Clinical Trial toolkit 28-Jan-2025  + (GBR Clinical Trial toolkit 28-Jan-2025)

• Document:GBR Clinical investigations of medical devices – compiling a submission to MHRA May 2021  + (GBR Clinical investigations of medical devices – compiling a submission to MHRA May 2021)
• Document:GBR Data Protection Act 2018 06-Jun-2022  + (GBR Data Protection Act 2018 06-Jun-2022)
• Document:GBR Directive 2001/20/EC 04-Apr-2001  + (GBR Directive 2001/20/EC 04-Apr-2001)
• Document:GBR Directive 90/385/EEC 05-Sep-2007  + (GBR Directive 90/385/EEC 05-Sep-2007)
• Document:GBR Directive 93/42/EEC 11-Oct-2007  + (GBR Directive 93/42/EEC 11-Oct-2007)
• Document:GBR Directive 98/79/EC 20-Dec-2011  + (GBR Directive 98/79/EC 20-Dec-2011)
• Document:GBR GUIDANCE FOR THE NOTIFICATION OF SERIOUS BREACHES OF GCP OR THE TRIAL PROTOCOL 08-Jul-2020  + (GBR GUIDANCE FOR THE NOTIFICATION OF SERIOUS BREACHES OF GCP OR THE TRIAL PROTOCOL 08-Jul-2020)
• Document:GBR Guidance Access to Electronic Health Records by Sponsor representatives in clinical trials 44447  + (GBR Guidance Access to Electronic Health Records by Sponsor representatives in clinical trials 44447)
• Document:GBR Guidance Managing clinical trials during Coronavirus (COVID-19) 16-Nov-.2021  + (GBR Guidance Managing clinical trials during Coronavirus (COVID-19) 16-Nov-.2021)
• Document:GBR Guidance - Good clinical practice for clinical trials 16-Oct-2015  + (GBR Guidance - Good clinical practice for clinical trials 16-Oct-2015)
• Document:GBR HRA - Ending your project 28-Jan-2025  + (GBR HRA - Ending your project 28-Jan-2025)
• Document:GBR IRAS - Integrated Research Application System 28-Jan-2025  + (GBR IRAS - Integrated Research Application System 28-Jan-2025)
• Document:GBR MEDDEV 2.7/3 revision 3 May-2015  + (GBR MEDDEV 2.7/3 revision 3 May-2015)
• Document:GBR MHRA GCP Inspection Dossier template V7.0  + (GBR MHRA GCP Inspection Dossier template V7.0)
• Document:GBR Making changes to a research study to manage the impact of COVID-19 12-Oct-2021  + (GBR Making changes to a research study to manage the impact of COVID-19 12-Oct-2021)
• Document:GBR Medicines and Medical Devices Act 2021 21-Feb-2021  + (GBR Medicines and Medical Devices Act 2021 21-Feb-2021)
• Document:GBR NHS: Records Management Code of Practice 07-Aug-2023  + (GBR NHS: Records Management Code of Practice 07-Aug-2023)
• Document:GBR NIHR - National Institute for Health and Care Research 28-Jan-2025  + (GBR NIHR - National Institute for Health and Care Research 28-Jan-2025)
• Document:GBR National Health Service Act 2006 02-Dec-2019  + (GBR National Health Service Act 2006 02-Dec-2019)
• Document:GBR The Electronic Identification and Trust Services for Electronic Transactions (Amendment etc.) (EU Exit) Regulations 2019 23-Jan-2019  + (GBR The Electronic Identification and Trust Services for Electronic Transactions (Amendment etc.) (EU Exit) Regulations 2019 23-Jan-2019)
• Document:GBR The Human Medicines Regulations 2012 01-Jan-2025  + (GBR The Human Medicines Regulations 2012 01-Jan-2025)
• Document:GBR The Medical Devices Regulations 2002 11-Feb-2021  + (GBR The Medical Devices Regulations 2002 11-Feb-2021)
• Document:GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004  + (GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004)
• Document:GBR UK GDPR - United Kingdom General Data Protection Regulation 31-Dec-2020  + (GBR UK GDPR - United Kingdom General Data Protection Regulation 31-Dec-2020)
• Document:ICH ICH E11 Guideline R1 (2017)  + (ICH ICH E11 Guideline R1 (2017))