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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 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))
• Document:ICH ICH E19 Guideline 2022  + (ICH ICH E19 Guideline 2022)
• Document:ICH ICH E21 Concept paper 2023  + (ICH ICH E21 Concept paper 2023)

• Document:ICH ICH E2A Guideline 1994  + (ICH ICH E2A Guideline 1994)

• Document:ICH ICH E2F Guideline 2010  + (ICH ICH E2F Guideline 2010)
• Document:ICH ICH E3 Guideline 1995  + (ICH ICH E3 Guideline 1995)
• Document:ICH ICH E6 Guideline - Annex 2 R3 Annex 2  + (ICH ICH E6 Guideline - Annex 2 R3 Annex 2)
• Document:ICH ICH E6 Guideline R3 (2025)  + (ICH ICH E6 Guideline R3 (2025))
• Document:ICH ICH E7 Guideline 1993  + (ICH ICH E7 Guideline 1993)
• Document:ICH ICH E8 Guideline R1 (2021)  + (ICH ICH E8 Guideline R1 (2021))
• Document:ICH ICH E9 Guideline 1998  + (ICH ICH E9 Guideline 1998)
• Document:ICH ICH E9 Guideline - Addendum R1 20-Nov-2019  + (ICH ICH E9 Guideline - Addendum R1 20-Nov-2019)
• Document:ICH ICH Guidelines -  + (ICH ICH Guidelines -)
• Document:IMDRF IMDRF – Guidelines -  + (IMDRF IMDRF – Guidelines -)
• Document:INT ISPE - GPP Revision 3 (2015)  + (INT ISPE - GPP Revision 3 (2015))
• Document:INT Nuremberg Code 1947  + (INT Nuremberg Code 1947)
• Document:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020  + (ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020)
• Document:N.A. (STROBE)statement: guidelines for reporting observational studies Apr-2008  + (N.A. (STROBE)statement: guidelines for reporting observational studies Apr-2008)
• Document:N.A. Article from Mora et al. 2023  + (N.A. Article from Mora et al. 2023)
• Document:N.A. Minimum Criteria for ICH E6 (R3) GCP Investigator Site Personnel Training V3.0  + (N.A. Minimum Criteria for ICH E6 (R3) GCP Investigator Site Personnel Training V3.0)
• Document:N.A. SPIRIT 2013 - Chan et al. 2013  + (N.A. SPIRIT 2013 - Chan et al. 2013)
• Document:N.A. Transcelerate GCP mutual recognition programm FAQ 21-May-2025  + (N.A. Transcelerate GCP mutual recognition programm FAQ 21-May-2025)
• Document:SMW Test  + (TEST-SMW-CHECK)
• Document:USA 21 CFR Part 11 09-Apr-2025  + (USA 21 CFR Part 11 09-Apr-2025)
• Document:USA 21 CFR Part 312 09-Apr-2025  + (USA 21 CFR Part 312 09-Apr-2025)
• Document:USA 21 CFR Part 314 09-Apr-2025  + (USA 21 CFR Part 314 09-Apr-2025)
• Document:USA 21 CFR Part 320 09-Apr-2025  + (USA 21 CFR Part 320 09-Apr-2025)
• Document:USA 21 CFR Part 50 09-Apr-2025  + (USA 21 CFR Part 50 09-Apr-2025)
• Document:USA 21 CFR Part 54 09-Apr-2025  + (USA 21 CFR Part 54 09-Apr-2025)