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Showing 20 pages using this property.
U
USA 21 CFR Part 56 09-Apr-2025 § 56.105 +
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USA 21 CFR Part 56 09-Apr-2025 § 56.109 +
EN  +
USA 21 CFR Part 56 09-Apr-2025 § 56.111 - §56.112 +
EN  +
USA 45 CFR Part 46 09-Apr-2025 § 46.124 +
EN  +
USA 21 CFR Part 312 09-Apr-2025 § 312.40 (b) +
EN  +
USA 21 CFR Part 812 09-Apr-2025 Subpart B +
EN  +
USA 21 CFR Part 812 09-Apr-2025 § 812.30 +
EN  +
USA 21 CFR Part 812 09-Apr-2025 § 812.42 +
EN  +
USA 21 CFR Part 812 09-Apr-2025 Subpart D +
EN  +
USA 42 CFR Part 11 09-Apr-2025 § 11.4 +
EN  +
USA 42 CFR Part 11 09-Apr-2025 § 11.6 +
EN  +
USA 42 CFR Part 11 09-Apr-2025 § 11.8 +
EN  +
USA 42 CFR Part 11 09-Apr-2025 § 11.24 +
EN  +
USA 42 CFR Part 11 09-Apr-2025 § 11.64 +
EN  +
I
ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 Annex E-001 +
EN  +
ICH ICH E6 Guideline R3 (2025) Appendix C-001 +
EN  +
ICH ICH E6 Guideline R3 (2025) Appendix C C.2.3 +
EN  +
E
EU EMA/INS/GCP/856758/ 2018 Guideline on the content, management and archiving of the clinical trial master file (paper and/or electronic) 06-Dec-2018 3 +
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EU EMA/INS/GCP/856758/ 2018 Guideline on the content, management and archiving of the clinical trial master file (paper and/or electronic) 06-Dec-2018 3.5.2 +
EN  +
EU EMA/INS/GCP/856758/ 2018 Guideline on the content, management and archiving of the clinical trial master file (paper and/or electronic) 06-Dec-2018 3.5.3 +
EN  +
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