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List of results
- Document:GBR Clinical investigations of medical devices – compiling a submission to MHRA May 2021 +
- Document:GBR Clinical Trial toolkit 28-Jan-2025 +
- Document:GBR Data Protection Act 2018 06-Jun-2022 +
- Document:GBR Directive 2001/20/EC 04-Apr-2001 +
- Document:GBR Directive 90/385/EEC 05-Sep-2007 +
- Document:GBR Directive 93/42/EEC 11-Oct-2007 +
- Document: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 +
- Document: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 +
- Document:GBR HRA - Ending your project 28-Jan-2025 +
- Document:GBR Guidance - Good clinical practice for clinical trials 16-Oct-2015 +
- Document:GBR IRAS - Integrated Research Application System 28-Jan-2025 +
- Document:GBR Making changes to a research study to manage the impact of COVID-19 12-Oct-2021 +
- Document:GBR MEDDEV 2.7/3 revision 3 May-2015 +
- Document:GBR Medicines and Medical Devices Act 2021 21-Feb-2021 +
- Document:GBR National Health Service Act 2006 02-Dec-2019 +
- Document:GBR NHS: Records Management Code of Practice 07-Aug-2023 +
- Document:GBR NIHR - National Institute for Health and Care Research 28-Jan-2025 +
- Document: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 +
- Document:GBR The Medical Devices Regulations 2002 11-Feb-2021 +
- Document: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 +
- Document:GBR MHRA GCP Inspection Dossier template V7.0 +