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- Document:ICH ICH E6 Guideline - Annex 2 R3 Annex 2 + (R3 Annex 2)
- Document:USA NIH - SCORE Manual: Appendix Source Documents Requirements Rev 01 16-Aug-2025 + (Rev 01 16-Aug-2025)
- Document:EU GVP: Module VIII EMA/813938/2011 Rev. 3 (2017) + (Rev. 3 (2017))
- Document:EU GVP: Module XVI EMA/204715/2012 Rev. 3 (2024) + (Rev. 3 (2024))
- Document:EU ENCePP - Guide on Methodological Standards in Pharmacoepidemiology Revision 11 (2023) + (Revision 11 (2023))
- Document:INT ISPE - GPP Revision 3 (2015) + (Revision 3 (2015))
- Document:USA FDA Guidance for Industry - Electronic Source Data in Clinical Investigations Sep-2013 + (Sep-2013)
- Document:N.A. Minimum Criteria for ICH E6 (R3) GCP Investigator Site Personnel Training V3.0 + (V3.0)
- Document:GBR MHRA GCP Inspection Dossier template V7.0 + (V7.0)
- Document:USA FDA - HUMAN DRUG CGMP NOTES Volume 8, Number 3 + (Volume 8, Number 3)
- Document:DEU Empfehlungen des BfArM und des PEI zur Europäischen Guidance during COVID-19 v4 04-Feb-2021 + (v4 04-Feb-2021)
- Document:EU GUIDANCE ON THE MANAGEMENT OF CLINICAL TRIALS DURING THE COVID-19 (CORONAVIRUS) PANDEMIC v5 10-Feb-2022 + (v5 10-Feb-2022)
- Document:USA CTCAE - Common Terminology Criteria for Adverse Events v5.0 (2017) + (v5.0 (2017))