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Showing 20 pages using this property.
I
ICH ICH E6 Guideline R3 (2025) Appendix B. B4 +
1.1.1  +
W
WHO WHO - Guidance for best practices for clinical trials 2024 1.1 - Clinical Research +
1.1.1  +
WHO WHO - Guidance for best practices for clinical trials 2024 1.4 +
1.1.1  +
I
ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 6.3 +
1.1.1  +
INT Nuremberg Code 1947 Code +
1.1.3  +
W
WMA Declaration of Helsinki 2024 - +
1.1.3  +
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - Good Clinical Practice (GCP) +
1.1.3  +
WHO WHO - HANDBOOK FOR GOOD CLINICAL RESEARCH PRACTICE (GCP) 2005 WHO Principles of GCP +
1.1.3  +
E
EUR European Bioethics Convention 1997 - +
1.1.3  +
I
ICH ICH E6 Guideline R3 (2025) I +
1.1.4  +
ICH ICH E6 Guideline R3 (2025) II +
1.1.4  +
ICH ICH E6 Guideline R3 (2025) GLOSSARY - Clinical Trial +
1.2.1  +
W
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - clinical trial +
1.2.1  +
I
ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 3.8 +
1.2.1  +
W
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - pharmaceutical product +
1.2.2  +
WHO WHO - Guidance for best practices for clinical trials 2024 1.1 - NIS +
1.2.2  +
I
ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 Annex I 6.3 +
1.2.2  +
E
EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 2 Paragraph 2 No. 1 +
1.2.2  +
EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 2 Paragraph 2 No. 2 +
1.2.2  +
EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 2 Paragraph 2 No. 3 +
1.2.2  +
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