Pages that link to "Template:DocumentData"

The following pages link to Template:DocumentData:

Displaying 50 items.

• Document:EU GVP: Module XVI EMA/204715/2012 Rev. 3 (2024) (transclusion) (← links)
• Document:EU INS/GCP/46309/2012 - Classification and analysis of the GCP inspection findings of GCP inspections conducted at the request of the CHMP 2012 (transclusion) (← links)
• Document:EU MDCG Guidelines - (transclusion) (← links)
• Document:EU Recommendations of the expert group - Risk proportionate approaches in clinical trials 25-Apr-2017 (transclusion) (← links)
• Document:EU Regulation (EC) No 726/2004 - authorisation and supervision of medicinal products for human use 28-Jan-22 (transclusion) (← links)
• Document:EU Regulation (EU) 2016/679 (GDPR) 04-May-2016 (transclusion) (← links)
• Document:EU Regulation (EU) 2017/745 - Medical Device Regulation 05-May-2017 Preamble (transclusion) (← links)
• Document:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 (transclusion) (← links)
• Document:EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 05-May-2017 Preamble (transclusion) (← links)
• Document:EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 (transclusion) (← links)
• Document:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 (transclusion) (← links)
• Document:EU Regulation (EU) 536/2014 - clinical trials 27-May-2014 Preamble (transclusion) (← links)
• Document:EU Regulation (EU) 910/2014 - electronic identification 17-Sep-2014 (transclusion) (← links)
• Document:EU Regulation (EU) No 520/2012 - performance of pharmacovigilance activities 20-Jun-12 (transclusion) (← links)
• Document:EU ; GBR MDCG 2020-10/1 - Safety reporting in clinical investigations of medical devices 2020 (transclusion) (← links)
• Document:EU ; GBR Regulation (EC) No 1223/2009 - Cosmetic Products 01-Dec-2023 (transclusion) (← links)
• Document:EU ; GBR Regulation (EC) No 178/2002 - Food Safety 01-Jul-2022 (transclusion) (← links)
• Document:EUR European Bioethics Convention 1997 (transclusion) (← links)
• Document:FRA AEC DOC010 V.04 01-Jun-2018 (transclusion) (← links)
• Document:FRA AEC DOC012 v03 Avis aux promoteurs d’investigations cliniques de DM (RIPH1) – Partie II 16-May-2025 (transclusion) (← links)
• Document:FRA AEC-DM-DMDIV DOC006 v04 AAP RDM Partie II Modalités pratiques 16-May-2025 (transclusion) (← links)
• Document:FRA Bonnes pratiques - CONTRÔLE QUALITÉ À DISTANCE DES ESSAIS CLINIQUES (CNIL) 16-May-2024 (transclusion) (← links)
• Document:FRA Code de la Santé Publique - Partie législative - 1ere partie, Livre 1er, Titre II 16-May-2025 (transclusion) (← links)
• Document:FRA Code de la Santé Publique - Partie Réglementaire - 1ere partie, Livre 1er, Titre II 16-May-2025 (transclusion) (← links)
• Document:FRA Constitution du 4 octobre 1958 10-Mar-2024 (transclusion) (← links)
• Document:FRA DHOS/E1/DAF/DPACI no 2007-322 14-Aug-2007 (transclusion) (← links)
• Document:FRA Guide de légistique 07-Feb-2024 (transclusion) (← links)
• Document:FRA Infographie - La hiérarchie des normes 22-Mar-2024 (transclusion) (← links)
• Document:FRA SI RIPH 2G - Website 16-May-2025 (transclusion) (← links)
• Document:FRA SURV VIG DOC118 V01 REC-Avis aux promoteurs -Partie V 16-May-2025 (transclusion) (← links)
• Document:GBR Clinical investigations of medical devices – compiling a submission to MHRA May 2021 (transclusion) (← links)
• Document:GBR Clinical Trial toolkit 28-Jan-2025 (transclusion) (← links)
• Document:GBR Data Protection Act 2018 06-Jun-2022 (transclusion) (← links)
• Document:GBR Directive 2001/20/EC 04-Apr-2001 (transclusion) (← links)
• Document:GBR Directive 90/385/EEC 05-Sep-2007 (transclusion) (← links)
• Document:GBR Directive 93/42/EEC 11-Oct-2007 (transclusion) (← links)
• Document:GBR Directive 98/79/EC 20-Dec-2011 (transclusion) (← links)
• Document:GBR GUIDANCE FOR THE NOTIFICATION OF SERIOUS BREACHES OF GCP OR THE TRIAL PROTOCOL 08-Jul-2020 (transclusion) (← links)
• Document:GBR Guidance Access to Electronic Health Records by Sponsor representatives in clinical trials 44447 (transclusion) (← links)
• Document:GBR Guidance Managing clinical trials during Coronavirus (COVID-19) 16-Nov-.2021 (transclusion) (← links)
• Document:GBR HRA - Ending your project 28-Jan-2025 (transclusion) (← links)
• Document:GBR Guidance - Good clinical practice for clinical trials 16-Oct-2015 (transclusion) (← links)
• Document:GBR IRAS - Integrated Research Application System 28-Jan-2025 (transclusion) (← links)
• Document:GBR Making changes to a research study to manage the impact of COVID-19 12-Oct-2021 (transclusion) (← links)
• Document:GBR MEDDEV 2.7/3 revision 3 May-2015 (transclusion) (← links)
• Document:GBR Medicines and Medical Devices Act 2021 21-Feb-2021 (transclusion) (← links)
• Document:GBR National Health Service Act 2006 02-Dec-2019 (transclusion) (← links)
• Document:GBR NHS: Records Management Code of Practice 07-Aug-2023 (transclusion) (← links)
• Document:GBR NIHR - National Institute for Health and Care Research 28-Jan-2025 (transclusion) (← links)
• Document:GBR The Electronic Identification and Trust Services for Electronic Transactions (Amendment etc.) (EU Exit) Regulations 2019 23-Jan-2019 (transclusion) (← links)