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• 13:49, 16 July 2026 Gxplex admin talk contribs imported Reference:USA 21 CFR Part 812 09-Apr-2025 § 812.43 by file upload (1 revision)
• 13:49, 16 July 2026 Gxplex admin talk contribs imported Reference:USA 21 CFR Part 812 09-Apr-2025 § 812.40 by file upload (1 revision)
• 13:49, 16 July 2026 Gxplex admin talk contribs imported Reference:USA 21 CFR Part 812 09-Apr-2025 § 812.3 (o) by file upload (1 revision)
• 13:49, 16 July 2026 Gxplex admin talk contribs imported Reference:USA 21 CFR Part 812 09-Apr-2025 § 812.3 (n) by file upload (1 revision)
• 13:49, 16 July 2026 Gxplex admin talk contribs imported Reference:USA 21 CFR Part 54 09-Apr-2025 § 54.4 list of investigators by file upload (1 revision)
• 13:49, 16 July 2026 Gxplex admin talk contribs imported Reference:USA 21 CFR Part 312 09-Apr-2025 § 312.53 by file upload (1 revision)
• 13:49, 16 July 2026 Gxplex admin talk contribs imported Reference:USA 21 CFR Part 312 09-Apr-2025 § 312.52 by file upload (1 revision)
• 13:49, 16 July 2026 Gxplex admin talk contribs imported Reference:USA 21 CFR Part 312 09-Apr-2025 § 312.50 by file upload (1 revision)
• 13:49, 16 July 2026 Gxplex admin talk contribs imported Reference:USA 21 CFR Part 312 09-Apr-2025 § 312.3 (b) - CRO by file upload (1 revision)
• 13:49, 16 July 2026 Gxplex admin talk contribs imported Reference:USA 21 CFR Part 312 09-Apr-2025 § 312.3 (b) - Sponsor-Investigator by file upload (1 revision)
• 13:49, 16 July 2026 Gxplex admin talk contribs imported Reference:USA 21 CFR Part 312 09-Apr-2025 § 312.3 (b) - Sponsor by file upload (1 revision)
• 13:49, 16 July 2026 Gxplex admin talk contribs imported Reference:USA 21 CFR Part 50 09-Apr-2025 § 50.3 (f) by file upload (1 revision)
• 13:49, 16 July 2026 Gxplex admin talk contribs imported Reference:USA 21 CFR Part 50 09-Apr-2025 § 50.3 (e) by file upload (1 revision)
• 13:49, 16 July 2026 Gxplex admin talk contribs imported Reference:GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 3 (6) - (11) by file upload (1 revision)
• 13:49, 16 July 2026 Gxplex admin talk contribs imported Reference:GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 3 (1) - (5) by file upload (1 revision)
• 13:49, 16 July 2026 Gxplex admin talk contribs imported Reference:DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 40b-002 by file upload (1 revision)
• 13:49, 16 July 2026 Gxplex admin talk contribs imported Reference:DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 4 Absatz 24 by file upload (1 revision)
• 13:49, 16 July 2026 Gxplex admin talk contribs imported Reference:EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Annex XIV Chapter II Section 2 by file upload (1 revision)
• 13:49, 16 July 2026 Gxplex admin talk contribs imported Reference:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Annex XV Chapter III 2. ; 7. by file upload (1 revision)
• 13:49, 16 July 2026 Gxplex admin talk contribs imported Reference:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 9 by file upload (1 revision)
• 13:49, 16 July 2026 Gxplex admin talk contribs imported Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 5 by file upload (1 revision)
• 13:49, 16 July 2026 Gxplex admin talk contribs imported Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 4.17 by file upload (1 revision)
• 13:49, 16 July 2026 Gxplex admin talk contribs imported Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - contract research organization (CRO) by file upload (1 revision)
• 13:49, 16 July 2026 Gxplex admin talk contribs imported Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - sponsor by file upload (1 revision)
• 13:49, 16 July 2026 Gxplex admin talk contribs imported Reference:ICH ICH E6 Guideline R3 (2025) III. Annex 1 3 by file upload (1 revision)
• 13:49, 16 July 2026 Gxplex admin talk contribs imported Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Sponsor-Investigator by file upload (1 revision)
• 13:49, 16 July 2026 Gxplex admin talk contribs imported Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Sponsor by file upload (1 revision)
• 13:49, 16 July 2026 Gxplex admin talk contribs imported Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Service Provider by file upload (1 revision)
• 13:49, 16 July 2026 Gxplex admin talk contribs imported Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Contract Research Organisation (CRO) by file upload (1 revision)
• 13:49, 16 July 2026 Gxplex admin talk contribs imported Reference:DEU DGEPi - GEP Guter Epidemiologischer Praxis Sep-2018 Leitlinie 3 3.10 by file upload (1 revision)
• 13:49, 16 July 2026 Gxplex admin talk contribs imported Reference:ICH ICH E6 Guideline R3 (2025) Appendix C-002 by file upload (1 revision)
• 13:49, 16 July 2026 Gxplex admin talk contribs imported Reference:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 Annex E-002 by file upload (1 revision)
• 13:49, 16 July 2026 Gxplex admin talk contribs imported Reference:USA 21 CFR Part 812 09-Apr-2025 § 812.27 by file upload (1 revision)
• 13:49, 16 July 2026 Gxplex admin talk contribs imported Reference:USA 21 CFR Part 312 09-Apr-2025 § 312.23 (a) ; (5) by file upload (1 revision)
• 13:49, 16 July 2026 Gxplex admin talk contribs imported Reference:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 Annex B by file upload (1 revision)
• 13:49, 16 July 2026 Gxplex admin talk contribs imported Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - investigator’s brochure by file upload (1 revision)
• 13:49, 16 July 2026 Gxplex admin talk contribs imported Reference:ICH ICH E6 Guideline R3 (2025) Appendix A by file upload (1 revision)
• 13:49, 16 July 2026 Gxplex admin talk contribs imported Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Investigator’s Brochure (IB) by file upload (1 revision)
• 13:49, 16 July 2026 Gxplex admin talk contribs imported Reference:USA 21 CFR Part 812 09-Apr-2025 § 812.25 by file upload (1 revision)
• 13:49, 16 July 2026 Gxplex admin talk contribs imported Reference:USA 21 CFR Part 312 09-Apr-2025 § 312.23 (a) ; (6) by file upload (1 revision)
• 13:49, 16 July 2026 Gxplex admin talk contribs imported Reference:DEU DGEPi - GEP Guter Epidemiologischer Praxis Sep-2018 Leitlinie 3 by file upload (1 revision)
• 13:49, 16 July 2026 Gxplex admin talk contribs imported Reference:EU ENCePP - Guide on Methodological Standards in Pharmacoepidemiology Revision 11 (2023) 3 by file upload (1 revision)
• 13:49, 16 July 2026 Gxplex admin talk contribs imported Reference:INT ISPE - GPP Revision 3 (2015) II. by file upload (1 revision)
• 13:49, 16 July 2026 Gxplex admin talk contribs imported Reference:EU GVP: Module VIII EMA/813938/2011 Rev. 3 (2017) - by file upload (1 revision)
• 13:49, 16 July 2026 Gxplex admin talk contribs imported Reference:EU Regulation (EU) No 520/2012 - performance of pharmacovigilance activities 20-Jun-12 Annex III 1. by file upload (1 revision)
• 13:49, 16 July 2026 Gxplex admin talk contribs imported Reference:EU EMA/298712/2022 - Complex clinical trials – Questions and answers 23-May-2022 Glossary by file upload (1 revision)
• 13:49, 16 July 2026 Gxplex admin talk contribs imported Reference:ICH ICH E8 Guideline R1 (2021) 5. by file upload (1 revision)
• 13:49, 16 July 2026 Gxplex admin talk contribs imported Reference:N.A. SPIRIT 2013 - Chan et al. 2013 - by file upload (1 revision)
• 13:49, 16 July 2026 Gxplex admin talk contribs imported Reference:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 Annex A - CIP by file upload (1 revision)
• 13:49, 16 July 2026 Gxplex admin talk contribs imported Reference:WHO WHO - HANDBOOK FOR GOOD CLINICAL RESEARCH PRACTICE (GCP) 2005 Page 28-29 by file upload (1 revision)