Main public logs

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 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"
• 16:49, 24 June 2026 Gxplex admin talk contribs set 305 as the approved revision for "USA 21 CFR Part 11 09-Apr-2025"
• 16:49, 24 June 2026 Gxplex admin talk contribs set 303 as the approved revision for "GBR UK GDPR - United Kingdom General Data Protection Regulation 31-Dec-2020"
• 16:49, 24 June 2026 Gxplex admin talk contribs set 301 as the approved revision for "GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004"
• 16:49, 24 June 2026 Gxplex admin talk contribs set 299 as the approved revision for "GBR The Medical Devices Regulations 2002 11-Feb-2021"
• 16:49, 24 June 2026 Gxplex admin talk contribs set 297 as the approved revision for "GBR The Human Medicines Regulations 2012 01-Jan-2025"
• 16:49, 24 June 2026 Gxplex admin talk contribs set 295 as the approved revision for "GBR The Electronic Identification and Trust Services for Electronic Transactions (Amendment etc.) (EU Exit) Regulations 2019 23-Jan-2019"
• 16:49, 24 June 2026 Gxplex admin talk contribs set 293 as the approved revision for "GBR NIHR - National Institute for Health and Care Research 28-Jan-2025"
• 16:49, 24 June 2026 Gxplex admin talk contribs set 291 as the approved revision for "GBR NHS: Records Management Code of Practice 07-Aug-2023"
• 16:49, 24 June 2026 Gxplex admin talk contribs set 289 as the approved revision for "GBR National Health Service Act 2006 02-Dec-2019"
• 16:49, 24 June 2026 Gxplex admin talk contribs set 287 as the approved revision for "GBR Medicines and Medical Devices Act 2021 21-Feb-2021"
• 16:49, 24 June 2026 Gxplex admin talk contribs set 285 as the approved revision for "GBR MEDDEV 2.7/3 revision 3 May-2015"
• 16:49, 24 June 2026 Gxplex admin talk contribs set 283 as the approved revision for "GBR Making changes to a research study to manage the impact of COVID-19 12-Oct-2021"
• 16:49, 24 June 2026 Gxplex admin talk contribs set 281 as the approved revision for "GBR IRAS - Integrated Research Application System 28-Jan-2025"
• 16:49, 24 June 2026 Gxplex admin talk contribs set 279 as the approved revision for "GBR Guidance - Good clinical practice for clinical trials 16-Oct-2015"
• 16:49, 24 June 2026 Gxplex admin talk contribs set 277 as the approved revision for "GBR HRA - Ending your project 28-Jan-2025"
• 16:49, 24 June 2026 Gxplex admin talk contribs set 275 as the approved revision for "GBR Guidance Managing clinical trials during Coronavirus (COVID-19) 16-Nov-.2021"
• 16:49, 24 June 2026 Gxplex admin talk contribs set 273 as the approved revision for "GBR Guidance Access to Electronic Health Records by Sponsor representatives in clinical trials 44447"
• 16:49, 24 June 2026 Gxplex admin talk contribs set 271 as the approved revision for "GBR GUIDANCE FOR THE NOTIFICATION OF SERIOUS BREACHES OF GCP OR THE TRIAL PROTOCOL 08-Jul-2020"