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).
- 15:28, 29 June 2026 Gxplex admin talk contribs imported Reference:DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 63 g Absatz 1 – 2 by file upload (1 revision)
- 15:28, 29 June 2026 Gxplex admin talk contribs imported Reference:DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 63 f Absatz 1 – 3 by file upload (1 revision)
- 15:28, 29 June 2026 Gxplex admin talk contribs imported Reference:DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 4 Absatz 34 by file upload (1 revision)
- 15:28, 29 June 2026 Gxplex admin talk contribs imported Reference:DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 4 Absatz 23 by file upload (1 revision)
- 15:28, 29 June 2026 Gxplex admin talk contribs imported Reference:EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 2 Paragraph 58 by file upload (1 revision)
- 15:28, 29 June 2026 Gxplex admin talk contribs imported Reference:EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 2 Paragraph 42 by file upload (1 revision)
- 15:28, 29 June 2026 Gxplex admin talk contribs imported Reference:EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 48 by file upload (1 revision)
- 15:28, 29 June 2026 Gxplex admin talk contribs imported Reference:EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 2 Paragraph 45 by file upload (1 revision)
- 15:28, 29 June 2026 Gxplex admin talk contribs imported Reference:EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 2 Paragraph 14 by file upload (1 revision)
- 15:28, 29 June 2026 Gxplex admin talk contribs imported Reference:EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 2 Paragraph 11 by file upload (1 revision)
- 15:28, 29 June 2026 Gxplex admin talk contribs imported Reference:EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 2 Paragraph 7 – 9 by file upload (1 revision)
- 15:28, 29 June 2026 Gxplex admin talk contribs imported Reference:EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 2 Paragraph 4 – 6 by file upload (1 revision)
- 15:28, 29 June 2026 Gxplex admin talk contribs imported Reference:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 2 Paragraph 62 by file upload (1 revision)
- 15:28, 29 June 2026 Gxplex admin talk contribs imported Reference:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 2 Paragraph 45 by file upload (1 revision)
- 15:28, 29 June 2026 Gxplex admin talk contribs imported Reference:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 52 by file upload (1 revision)
- 15:28, 29 June 2026 Gxplex admin talk contribs imported Reference:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 2 Paragraph 46 by file upload (1 revision)
- 15:28, 29 June 2026 Gxplex admin talk contribs imported Reference:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 2 Paragraph 14 by file upload (1 revision)
- 15:28, 29 June 2026 Gxplex admin talk contribs imported Reference:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 2 Paragraph 10 – 12 by file upload (1 revision)
- 15:28, 29 June 2026 Gxplex admin talk contribs imported Reference:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 2 Paragraph 4 – 8 by file upload (1 revision)
- 15:28, 29 June 2026 Gxplex admin talk contribs imported Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 2 Paragraph 2 No. 4 by file upload (1 revision)
- 15:28, 29 June 2026 Gxplex admin talk contribs imported Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 2 Paragraph 2 No. 3 by file upload (1 revision)
- 15:28, 29 June 2026 Gxplex admin talk contribs imported Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 2 Paragraph 2 No. 2 by file upload (1 revision)
- 15:28, 29 June 2026 Gxplex admin talk contribs imported Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 2 Paragraph 2 No. 1 by file upload (1 revision)
- 15:28, 29 June 2026 Gxplex admin talk contribs imported Reference:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 Annex I 6.3 by file upload (1 revision)
- 15:28, 29 June 2026 Gxplex admin talk contribs imported Reference:WHO WHO - Guidance for best practices for clinical trials 2024 1.1 - NIS by file upload (1 revision)
- 15:28, 29 June 2026 Gxplex admin talk contribs imported Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - pharmaceutical product by file upload (1 revision)
- 15:28, 29 June 2026 Gxplex admin talk contribs imported Reference:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 3.8 by file upload (1 revision)
- 15:28, 29 June 2026 Gxplex admin talk contribs imported Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - clinical trial by file upload (1 revision)
- 15:28, 29 June 2026 Gxplex admin talk contribs imported Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Clinical Trial by file upload (1 revision)
- 15:28, 29 June 2026 Gxplex admin talk contribs imported Reference:ICH ICH E6 Guideline R3 (2025) II by file upload (1 revision)
- 15:28, 29 June 2026 Gxplex admin talk contribs imported Reference:ICH ICH E6 Guideline R3 (2025) I by file upload (1 revision)
- 15:28, 29 June 2026 Gxplex admin talk contribs imported Reference:EUR European Bioethics Convention 1997 - by file upload (1 revision)
- 15:28, 29 June 2026 Gxplex admin talk contribs imported Reference:WHO WHO - HANDBOOK FOR GOOD CLINICAL RESEARCH PRACTICE (GCP) 2005 WHO Principles of GCP by file upload (1 revision)
- 15:28, 29 June 2026 Gxplex admin talk contribs imported Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - Good Clinical Practice (GCP) by file upload (1 revision)
- 15:28, 29 June 2026 Gxplex admin talk contribs imported Reference:WMA Declaration of Helsinki 2024 - by file upload (1 revision)
- 15:28, 29 June 2026 Gxplex admin talk contribs imported Reference:INT Nuremberg Code 1947 Code by file upload (1 revision)
- 15:28, 29 June 2026 Gxplex admin talk contribs imported Reference:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 6.3 by file upload (1 revision)
- 15:28, 29 June 2026 Gxplex admin talk contribs imported Reference:WHO WHO - Guidance for best practices for clinical trials 2024 1.4 by file upload (1 revision)
- 15:28, 29 June 2026 Gxplex admin talk contribs imported Reference:WHO WHO - Guidance for best practices for clinical trials 2024 1.1 - Clinical Research by file upload (1 revision)
- 15:28, 29 June 2026 Gxplex admin talk contribs imported Reference:ICH ICH E6 Guideline R3 (2025) Appendix B. B4 by file upload (1 revision)
- 15:28, 29 June 2026 Gxplex admin talk contribs imported Document:USA WARNING LETTER - Purolea Cosmetics Lab MARCS-CMS 722591 46114 by file upload (1 revision)
- 15:28, 29 June 2026 Gxplex admin talk contribs imported Document:GBR MHRA GCP Inspection Dossier template V7.0 by file upload (1 revision)
- 15:28, 29 June 2026 Gxplex admin talk contribs imported Document:N.A. Transcelerate GCP mutual recognition programm FAQ 21-May-2025 by file upload (1 revision)
- 15:28, 29 June 2026 Gxplex admin talk contribs imported Document:N.A. Minimum Criteria for ICH E6 (R3) GCP Investigator Site Personnel Training V3.0 by file upload (1 revision)
- 15:28, 29 June 2026 Gxplex admin talk contribs imported Document:WHO WHO Good Practices for Clinical Trial Design and Implementation 04-May-2026 by file upload (1 revision)
- 15:28, 29 June 2026 Gxplex admin talk contribs imported Document:EU European Medicines Agency’s Data Protection: Notice For Microsoft (MS) Copilot 365 - EMA pilot phase ; EMA/216030/2025 45838 by file upload (1 revision)
- 15:28, 29 June 2026 Gxplex admin talk contribs imported Document:DEU Deutsches Ärzteblatt 45849 by file upload (1 revision)
- 15:28, 29 June 2026 Gxplex admin talk contribs imported Document:DEU Richtlinie zur Bewertung der Qualifikation von Prüfern, Hauptprüfern, Leitern und ärztlichen Mitgliedern von Prüfungsteams durch Ethik-Kommissionen von Arbeitskreis Medizinischer Ethik-Kommissionen in der Bundesrepublik Deutschland e. V. und by file upload (1 revision)
- 15:28, 29 June 2026 Gxplex admin talk contribs imported Document:WMA Declaration of Helsinki 2024 by file upload (1 revision)
- 15:28, 29 June 2026 Gxplex admin talk contribs imported Document:WHO World Health Organization - by file upload (1 revision)