Pages that link to "Glossary:TAG-00124-Cas-Prü"

The following pages link to Glossary:TAG-00124-Cas-Prü:

Displaying 17 items.

• Glossary (← links)
• Reference:ICH ICH E6 Guideline R3 (2025) III. Annex 1 2.12.5 – 2.12.9 (← links)
• Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - patient/subject file (← links)
• Reference:USA 21 CFR Part 312 09-Apr-2025 § 312.62 (b) (← links)
• Reference:USA 21 CFR Part 812 09-Apr-2025 § 812.140 (a) (3) (← links)
• Reference:WHO WHO - Guidance for best practices for clinical trials 2024 2.1.8 (← links)
• Reference:AUT BASG - FAQ 11-Feb-2025 Schwarz (← links)
• Reference:USA FDA Guidance for Industry - Electronic Source Data in Clinical Investigations Sep-2013 III 2. (← links)
• Reference:USA NIH - SCORE Manual: Appendix Source Documents Requirements Rev 01 16-Aug-2025 Page 3 - CRF (← links)
• Reference:USA NIH - SCORE Manual: Appendix Source Documents Requirements Rev 01 16-Aug-2025 Page 3 - Note (← links)
• Reference:USA FDA Guidance for Industry - Electronic Source Data in Clinical Investigations Sep-2013 III 4. (← links)
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Case Report Form (CRF) (← links)
• Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - case -report form (CRF) (← links)
• Reference:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 6.6 (← links)
• Reference:DEU DGEPi - GEP Guter Epidemiologischer Praxis Sep-2018 Leitlinie 6 6.8 (← links)
• Reference:USA 21 CFR Part 314 09-Apr-2025 § 314.50 (← links)
• Reference:USA FDA Guidance for Industry - Oversight of Clinical Investigations — A Risk-Based Approach to Monitoring Aug-2013 III B. 3. (← links)