Pages that link to "Glossary:TAG-00252-Exp-hle"

The following pages link to Glossary:TAG-00252-Exp-hle:

Displaying 16 items.

• Glossary (← links)
• Reference:EU 2011/C 172/01 - CT-3 11-Jun-2011 Section 7 7.3.1 (← links)
• Reference:USA NCI GUIDELINES FOR INVESTIGATORS: ADVERSE EVENT REPORTING REQUIREMENTS FOR DCTD (CTEP AND CIP) INDs AND IDEs 30-Aug-2024 2.1.14. (← links)
• Reference:USA NCI GUIDELINES FOR INVESTIGATORS: ADVERSE EVENT REPORTING REQUIREMENTS FOR DCTD (CTEP AND CIP) INDs AND IDEs 30-Aug-2024 5.2 (← links)
• Reference:ICH ICH E2A Guideline 1994 III A. 2. (← links)
• Reference:EU 2011/C 172/01 - CT-3 11-Jun-2011 Section 7 7.3.3 (← links)
• Reference:USA FDA Guidance for Clinical Investigators, Sponsors, and IRBs Adverse Event Reporting to IRBs — Improving Human Subject Protection Jan-2009 Introduction ; III. B. ; IV. (← links)
• Reference:USA NCI GUIDELINES FOR INVESTIGATORS: ADVERSE EVENT REPORTING REQUIREMENTS FOR DCTD (CTEP AND CIP) INDs AND IDEs 30-Aug-2024 4.3 (← links)
• Reference:USA NCI GUIDELINES FOR INVESTIGATORS: ADVERSE EVENT REPORTING REQUIREMENTS FOR DCTD (CTEP AND CIP) INDs AND IDEs 30-Aug-2024 Appendix 1 (← links)
• Reference:USA NCI GUIDELINES FOR INVESTIGATORS: ADVERSE EVENT REPORTING REQUIREMENTS FOR DCTD (CTEP AND CIP) INDs AND IDEs 30-Aug-2024 5.3.1 (← links)
• Reference:USA NCI GUIDELINES FOR INVESTIGATORS: ADVERSE EVENT REPORTING REQUIREMENTS FOR DCTD (CTEP AND CIP) INDs AND IDEs 30-Aug-2024 5.3.2 (← links)
• Reference:ICH ICH E2A Guideline 1994 III B. - III C. (← links)
• Reference:ICH ICH E2A Guideline 1994 III E (← links)
• Reference:ICH ICH E6 Guideline R3 (2025) III. Annex 1 3.13.2 (c) (← links)
• Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 42 (← links)
• Reference:USA 21 CFR Part 312 09-Apr-2025 § 312.32 (c) (← links)