Pages that link to "Property:RefLanguage"

The following pages link to Property:RefLanguage:

Displaying 50 items.

• Document:EU ; GBR Regulation (EC) No 178/2002 - Food Safety 01-Jul-2022 (← links)
• Document:EUR European Bioethics Convention 1997 (← links)
• Document:FRA AEC DOC010 V.04 01-Jun-2018 (← links)
• Document:FRA AEC DOC012 v03 Avis aux promoteurs d’investigations cliniques de DM (RIPH1) – Partie II 16-May-2025 (← links)
• Document:FRA AEC-DM-DMDIV DOC006 v04 AAP RDM Partie II Modalités pratiques 16-May-2025 (← links)
• Document:FRA Bonnes pratiques - CONTRÔLE QUALITÉ À DISTANCE DES ESSAIS CLINIQUES (CNIL) 16-May-2024 (← links)
• Document:FRA Code de la Santé Publique - Partie législative - 1ere partie, Livre 1er, Titre II 16-May-2025 (← links)
• Document:FRA Code de la Santé Publique - Partie Réglementaire - 1ere partie, Livre 1er, Titre II 16-May-2025 (← links)
• Document:FRA Constitution du 4 octobre 1958 10-Mar-2024 (← links)
• Document:FRA DHOS/E1/DAF/DPACI no 2007-322 14-Aug-2007 (← links)
• Document:FRA Guide de légistique 07-Feb-2024 (← links)
• Document:FRA Infographie - La hiérarchie des normes 22-Mar-2024 (← links)
• Document:FRA SI RIPH 2G - Website 16-May-2025 (← links)
• Document:FRA SURV VIG DOC118 V01 REC-Avis aux promoteurs -Partie V 16-May-2025 (← links)
• Document:GBR Clinical investigations of medical devices – compiling a submission to MHRA May 2021 (← links)
• Document:GBR Data Protection Act 2018 06-Jun-2022 (← links)
• Document:GBR Directive 2001/20/EC 04-Apr-2001 (← links)
• Document:GBR Directive 93/42/EEC 11-Oct-2007 (← links)
• Document:GBR GUIDANCE FOR THE NOTIFICATION OF SERIOUS BREACHES OF GCP OR THE TRIAL PROTOCOL 08-Jul-2020 (← links)
• Document:GBR Guidance Access to Electronic Health Records by Sponsor representatives in clinical trials 44447 (← links)
• Document:GBR Guidance Managing clinical trials during Coronavirus (COVID-19) 16-Nov-.2021 (← links)
• Document:GBR HRA - Ending your project 28-Jan-2025 (← links)
• Document:GBR Guidance - Good clinical practice for clinical trials 16-Oct-2015 (← links)
• Document:GBR IRAS - Integrated Research Application System 28-Jan-2025 (← links)
• Document:GBR Making changes to a research study to manage the impact of COVID-19 12-Oct-2021 (← links)
• Document:GBR MEDDEV 2.7/3 revision 3 May-2015 (← links)
• Document:GBR Medicines and Medical Devices Act 2021 21-Feb-2021 (← links)
• Document:GBR NHS: Records Management Code of Practice 07-Aug-2023 (← links)
• Document:GBR NIHR - National Institute for Health and Care Research 28-Jan-2025 (← links)
• Document:GBR The Electronic Identification and Trust Services for Electronic Transactions (Amendment etc.) (EU Exit) Regulations 2019 23-Jan-2019 (← links)
• Document:GBR The Human Medicines Regulations 2012 01-Jan-2025 (← links)
• Document:GBR The Medical Devices Regulations 2002 11-Feb-2021 (← links)
• Document:GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 (← links)
• Document:GBR UK GDPR - United Kingdom General Data Protection Regulation 31-Dec-2020 (← links)
• Document:USA 21 CFR Part 11 09-Apr-2025 (← links)
• Document:USA 21 CFR Part 312 09-Apr-2025 (← links)
• Document:USA 21 CFR Part 314 09-Apr-2025 (← links)
• Document:USA 21 CFR Part 320 09-Apr-2025 (← links)
• Document:USA 21 CFR Part 50 09-Apr-2025 (← links)
• Document:USA 21 CFR Part 54 09-Apr-2025 (← links)
• Document:USA 21 CFR Part 56 09-Apr-2025 (← links)
• Document:USA 21 CFR Part 809 06-May-2024 (← links)
• Document:USA 21 CFR Part 812 09-Apr-2025 (← links)
• Document:USA 42 CFR Part 11 09-Apr-2025 (← links)
• Document:USA 45 CFR Part 160 09-Apr-2025 (← links)
• Document:USA 45 CFR Part 46 09-Apr-2025 (← links)
• 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 (← links)
• Document:USA CTCAE - Common Terminology Criteria for Adverse Events v5.0 (2017) (← links)
• Document:USA Expedited Review: Categories of Research that may be Reviewed Through an Expedited Review Procedure 1998 (← links)
• Document:USA FD&C Act - Federal Food, Drug, and Cosmetic Act 30-Sep-2023 (← links)