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 405 as the approved revision for "ICH ICH Guidelines -"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 403 as the approved revision for "ICH ICH E9 Guideline 1998"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 401 as the approved revision for "ICH ICH E9 Guideline - Addendum R1 20-Nov-2019"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 399 as the approved revision for "ICH ICH E8 Guideline R1 (2021)"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 397 as the approved revision for "ICH ICH E7 Guideline 1993"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 395 as the approved revision for "ICH ICH E6 Guideline - Annex 2 R3 Annex 2"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 393 as the approved revision for "ICH ICH E6 Guideline R3 (2025)"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 391 as the approved revision for "ICH ICH E3 Guideline 1995"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 389 as the approved revision for "ICH ICH E2F Guideline 2010"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 387 as the approved revision for "ICH ICH E2A Guideline 1994"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 385 as the approved revision for "ICH ICH E21 Concept paper 2023"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 383 as the approved revision for "ICH ICH E19 Guideline 2022"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 381 as the approved revision for "ICH ICH E11 Guideline R1 (2017)"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 379 as the approved revision for "CIOMS CIOMS Publications -"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 377 as the approved revision for "CIOMS CIOMS - International Ethical Guidelines for Health-related Research Involving Humans 2016"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 375 as the approved revision for "CIOMS CIOMS - International Ethical Guidelines for Biomedical Research Involving Human Subjects 2016"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 373 as the approved revision for "USA U.S. Code Title 21 30-Sep-2023"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 371 as the approved revision for "USA Recognized Consensus Standards - ISO 14155 21-Dec-2020"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 369 as the approved revision for "USA Recognized Consensus Standards N.A."
- 16:49, 24 June 2026 Gxplex admin talk contribs set 367 as the approved revision for "USA NIH - SCORE Manual: Appendix Source Documents Requirements Rev 01 16-Aug-2025"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 365 as the approved revision for "USA NIH - SCORE Manual N.A."
- 16:49, 24 June 2026 Gxplex admin talk contribs set 363 as the approved revision for "USA NCI GUIDELINES FOR INVESTIGATORS: ADVERSE EVENT REPORTING REQUIREMENTS FOR DCTD (CTEP AND CIP) INDs AND IDEs 30-Aug-2024"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 361 as the approved revision for "USA Informed Consent - FDA Guidance for IRBs, Clinical Investigators, and Sponsors Aug-2023"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 359 as the approved revision for "USA FDA Information - Observations and citations 20-Mar-2024"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 357 as the approved revision for "USA NIH - Glossary 27-May-2025"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 355 as the approved revision for "USA FDA INFORMATION SHEET - Recruiting Study Subjects, Guidance for Institutional Review Boards and Clinical Investigators Jan-1998"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 353 as the approved revision for "USA FDA Guidance for Industry Investigator Responsibilities — Protecting the Rights, Safety, and Welfare of Study Subjects Oct-2009"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 351 as the approved revision for "USA FDA Guidance for Industry - Oversight of Clinical Investigations — A Risk-Based Approach to Monitoring Aug-2013"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 349 as the approved revision for "USA FDA Guidance for Industry - Electronic Source Data in Clinical Investigations Sep-2013"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 347 as the approved revision for "USA FDA Guidance for Industry - Conduct of Clinical Trials of Medical Products During the COVID-19 Public Health Emergency Mar-2020"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 345 as the approved revision for "USA FDA Guidance for Industry - Computerized Systems Used in Clinical Trials 13-Apr-2015"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 343 as the approved revision for "USA FDA Guidance for Industry - Computerized Systems Used in Clinical Investigations May-2007"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 341 as the approved revision for "USA FDA Guidance for Clinical Investigators, Sponsors, and IRBs Adverse Event Reporting to IRBs — Improving Human Subject Protection Jan-2009"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 339 as the approved revision for "USA FDA - HUMAN DRUG CGMP NOTES Volume 8, Number 3"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 337 as the approved revision for "USA FDA - E6(R2) Good Clinical Practice: Integrated Addendum to ICH E6(R1): Guidance for Industry March 2018"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 335 as the approved revision for "USA FD&C Act - Federal Food, Drug, and Cosmetic Act 30-Sep-2023"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 333 as the approved revision for "USA Expedited Review: Categories of Research that may be Reviewed Through an Expedited Review Procedure 1998"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 331 as the approved revision for "USA CTCAE - Common Terminology Criteria for Adverse Events v5.0 (2017)"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 329 as the approved revision for "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"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 327 as the approved revision for "USA 45 CFR Part 46 09-Apr-2025"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 325 as the approved revision for "USA 45 CFR Part 160 09-Apr-2025"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 323 as the approved revision for "USA 42 CFR Part 11 09-Apr-2025"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 321 as the approved revision for "USA 21 CFR Part 812 09-Apr-2025"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 319 as the approved revision for "USA 21 CFR Part 809 06-May-2024"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 317 as the approved revision for "USA 21 CFR Part 56 09-Apr-2025"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 315 as the approved revision for "USA 21 CFR Part 54 09-Apr-2025"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 313 as the approved revision for "USA 21 CFR Part 50 09-Apr-2025"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 311 as the approved revision for "USA 21 CFR Part 320 09-Apr-2025"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 309 as the approved revision for "USA 21 CFR Part 314 09-Apr-2025"
- 16:49, 24 June 2026 Gxplex admin talk contribs set 307 as the approved revision for "USA 21 CFR Part 312 09-Apr-2025"