Main public logs
From GxPlex
Combined display of all available logs of GxPlex. You can narrow down the view by selecting a log type, the username (case-sensitive), or the affected page (also case-sensitive).
- 16:49, 24 June 2026 Gxplex admin talk contribs set 269 as the approved revision for "GBR Directive 98/79/EC 20-Dec-2011"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 267 as the approved revision for "GBR Directive 93/42/EEC 11-Oct-2007"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 265 as the approved revision for "GBR Directive 90/385/EEC 05-Sep-2007"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 263 as the approved revision for "GBR Directive 2001/20/EC 04-Apr-2001"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 261 as the approved revision for "GBR Data Protection Act 2018 06-Jun-2022"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 259 as the approved revision for "GBR Clinical Trial toolkit 28-Jan-2025"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 257 as the approved revision for "GBR Clinical investigations of medical devices – compiling a submission to MHRA May 2021"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 255 as the approved revision for "FRA SURV VIG DOC118 V01 REC-Avis aux promoteurs -Partie V 16-May-2025"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 253 as the approved revision for "FRA SI RIPH 2G - Website 16-May-2025"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 251 as the approved revision for "FRA Infographie - La hiérarchie des normes 22-Mar-2024"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 249 as the approved revision for "FRA Guide de légistique 07-Feb-2024"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 247 as the approved revision for "FRA DHOS/E1/DAF/DPACI no 2007-322 14-Aug-2007"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 245 as the approved revision for "FRA Constitution du 4 octobre 1958 10-Mar-2024"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 243 as the approved revision for "FRA Code de la Santé Publique - Partie Réglementaire - 1ere partie, Livre 1er, Titre II 16-May-2025"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 241 as the approved revision for "FRA Code de la Santé Publique - Partie législative - 1ere partie, Livre 1er, Titre II 16-May-2025"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 239 as the approved revision for "FRA Bonnes pratiques - CONTRÔLE QUALITÉ À DISTANCE DES ESSAIS CLINIQUES (CNIL) 16-May-2024"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 237 as the approved revision for "FRA AEC-DM-DMDIV DOC006 v04 AAP RDM Partie II Modalités pratiques 16-May-2025"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 235 as the approved revision for "FRA AEC DOC012 v03 Avis aux promoteurs d’investigations cliniques de DM (RIPH1) – Partie II 16-May-2025"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 233 as the approved revision for "FRA AEC DOC010 V.04 01-Jun-2018"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 231 as the approved revision for "EUR European Bioethics Convention 1997"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 229 as the approved revision for "EU ; GBR Regulation (EC) No 178/2002 - Food Safety 01-Jul-2022"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 227 as the approved revision for "EU ; GBR Regulation (EC) No 1223/2009 - Cosmetic Products 01-Dec-2023"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 225 as the approved revision for "EU ; GBR MDCG 2020-10/1 - Safety reporting in clinical investigations of medical devices 2020"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 223 as the approved revision for "EU Regulation (EU) No 520/2012 - performance of pharmacovigilance activities 20-Jun-12"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 221 as the approved revision for "EU Regulation (EU) 910/2014 - electronic identification 17-Sep-2014"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 219 as the approved revision for "EU Regulation (EU) 536/2014 - clinical trials 27-May-2014 Preamble"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 217 as the approved revision for "EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 215 as the approved revision for "EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 213 as the approved revision for "EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 05-May-2017 Preamble"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 211 as the approved revision for "EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 209 as the approved revision for "EU Regulation (EU) 2017/745 - Medical Device Regulation 05-May-2017 Preamble"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 207 as the approved revision for "EU Regulation (EU) 2016/679 (GDPR) 04-May-2016"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 205 as the approved revision for "EU Regulation (EC) No 726/2004 - authorisation and supervision of medicinal products for human use 28-Jan-22"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 203 as the approved revision for "EU Recommendations of the expert group - Risk proportionate approaches in clinical trials 25-Apr-2017"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 201 as the approved revision for "EU MDCG Guidelines -"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 199 as the approved revision for "EU INS/GCP/46309/2012 - Classification and analysis of the GCP inspection findings of GCP inspections conducted at the request of the CHMP 2012"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 197 as the approved revision for "EU GVP: Module XVI EMA/204715/2012 Rev. 3 (2024)"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 195 as the approved revision for "EU GVP: Module VIII EMA/813938/2011 Rev. 3 (2017)"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 193 as the approved revision for "EU GUIDANCE ON THE MANAGEMENT OF CLINICAL TRIALS DURING THE COVID-19 (CORONAVIRUS) PANDEMIC v5 10-Feb-2022"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 191 as the approved revision for "EU Eudralex - volume 4 GMP Guidelines Chapter 4 Jan-2011"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 189 as the approved revision for "EU Eudralex - volume 4 GMP Guidelines Annex 11 Jan-2011"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 187 as the approved revision for "EU EudraLex – Volume 10 -"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 185 as the approved revision for "EU ENCePP - Guide on Methodological Standards in Pharmacoepidemiology Revision 11 (2023)"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 183 as the approved revision for "EU EMEA/CHMP/313666/2005 - GUIDELINE ON THE EXPOSURE TO MEDICINAL PRODUCTS DURING PREGNANCY: NEED FOR POST-AUTHORISATION DATA 14-Nov-2005"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 181 as the approved revision for "EU EMA/INS/GCP/856758/ 2018 Guideline on the content, management and archiving of the clinical trial master file (paper and/or electronic) 06-Dec-2018"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 179 as the approved revision for "EU EMA/INS/GCP/143492/2022 - ANNEX I TO PROCEDURE FOR CONDUCTING GCP INSPECTIONS REQUESTED BY THE CHMP: INVESTIGATOR SITE 2022"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 177 as the approved revision for "EU EMA/INS/GCP/126568/2023 - Annual Report of the Good Clinical Practice (GCP) Inspectors' Working Group (IWG) 2022 2023"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 175 as the approved revision for "EU EMA/INS/GCP/112288/2023 - Guideline on computerised systems and electronic data in clinical trials 2023"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 173 as the approved revision for "EU EMA/786433/2022 Annex V – to guidance for the conduct of good clinical practice inspections – Phase I units 15-Nov-2022"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 171 as the approved revision for "EU EMA/698382/2021 - Guideline for the notification of serious breaches of Regulation (EU) No 536/2014 or the clinical trial protocol 2021"