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Glossary:TAG-00320-Foo-eri

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Glossary > FDA

FDA
Tag-ID TAG-00320-Foo-eri
English Food and Drug Administration
EN Abbr. FDA
French Food and Drug Administration / Agence américaine des aliments et médicaments
FR Abbr. FDA
German Food and Drug Administration / Amerikanische Arzneimittelbehörde
DE Abbr. FDA

References

 ScopeDocument partLanguageDocument
USA 21 CFR Part 11 09-Apr-2025 § 11.100G§ 11.100ENUSA 21 CFR Part 11 09-Apr-2025
USA 21 CFR Part 11 09-Apr-2025 § 11.200G§ 11.200ENUSA 21 CFR Part 11 09-Apr-2025
USA 21 CFR Part 11 09-Apr-2025 § 11.30G§ 11.30ENUSA 21 CFR Part 11 09-Apr-2025
USA 21 CFR Part 312 09-Apr-2025 § 312.53 (c)HM§ 312.53 (c)ENUSA 21 CFR Part 312 09-Apr-2025
USA 21 CFR Part 312 09-Apr-2025 § 312.58HM§ 312.58ENUSA 21 CFR Part 312 09-Apr-2025
USA 21 CFR Part 312 09-Apr-2025 § 312.68HM§ 312.68ENUSA 21 CFR Part 312 09-Apr-2025
USA 21 CFR Part 312 09-Apr-2025 § 312.70HM§ 312.70ENUSA 21 CFR Part 312 09-Apr-2025
USA 21 CFR Part 312 09-Apr-2025 § 312.85HM§ 312.85ENUSA 21 CFR Part 312 09-Apr-2025
USA 21 CFR Part 320 09-Apr-2025 § 320.22HM§ 320.22ENUSA 21 CFR Part 320 09-Apr-2025
USA 21 CFR Part 50 09-Apr-2025 § 50.20G§ 50.20ENUSA 21 CFR Part 50 09-Apr-2025
USA 21 CFR Part 50 09-Apr-2025 § 50.25 (a) - (b)G§ 50.25 (a) - (b)ENUSA 21 CFR Part 50 09-Apr-2025
USA 21 CFR Part 50 09-Apr-2025 § 50.25 (e)G§ 50.25 (e)ENUSA 21 CFR Part 50 09-Apr-2025
USA 21 CFR Part 50 09-Apr-2025 § 50.3G§ 50.3ENUSA 21 CFR Part 50 09-Apr-2025
USA 21 CFR Part 54 09-Apr-2025 § 54.1-001G§ 54.1ENUSA 21 CFR Part 54 09-Apr-2025
USA 21 CFR Part 54 09-Apr-2025 § 54.1-002G§ 54.1ENUSA 21 CFR Part 54 09-Apr-2025
USA 21 CFR Part 54 09-Apr-2025 § 54.4 disclosureG§ 54.4 disclosureENUSA 21 CFR Part 54 09-Apr-2025
USA 21 CFR Part 54 09-Apr-2025 § 54.4 list of investigatorsG§ 54.4 list of investigatorsENUSA 21 CFR Part 54 09-Apr-2025
USA 21 CFR Part 54 09-Apr-2025 § 54.6G§ 54.6ENUSA 21 CFR Part 54 09-Apr-2025
USA 21 CFR Part 56 09-Apr-2025 -G-ENUSA 21 CFR Part 56 09-Apr-2025
USA 21 CFR Part 56 09-Apr-2025 § 56.104G§ 56.104ENUSA 21 CFR Part 56 09-Apr-2025
USA 21 CFR Part 56 09-Apr-2025 § 56.104 (d)G§ 56.104 (d)ENUSA 21 CFR Part 56 09-Apr-2025
USA 21 CFR Part 56 09-Apr-2025 § 56.105G§ 56.105ENUSA 21 CFR Part 56 09-Apr-2025
USA 21 CFR Part 56 09-Apr-2025 § 56.110 (a) - (b) (1)G§ 56.110 (a) - (b) (1)ENUSA 21 CFR Part 56 09-Apr-2025
USA 21 CFR Part 812 09-Apr-2025 § 812.145MD§ 812.145ENUSA 21 CFR Part 812 09-Apr-2025
USA 21 CFR Part 812 09-Apr-2025 § 812.30MD§ 812.30ENUSA 21 CFR Part 812 09-Apr-2025
USA 21 CFR Part 812 09-Apr-2025 § 812.42MD§ 812.42ENUSA 21 CFR Part 812 09-Apr-2025
USA 21 CFR Part 812 09-Apr-2025 § 812.43 (c) (4)MD§ 812.43 (c) (4)ENUSA 21 CFR Part 812 09-Apr-2025
USA 21 CFR Part 812 09-Apr-2025 § 812.43 (c) (5)MD§ 812.43 (c) (5)ENUSA 21 CFR Part 812 09-Apr-2025
USA 45 CFR Part 160 09-Apr-2025 § 164.512G§ 164.512ENUSA 45 CFR Part 160 09-Apr-2025
USA FDA - E6(R2) Good Clinical Practice: Integrated Addendum to ICH E6(R1): Guidance for Industry March 2018 -G-ENUSA FDA - E6(R2) Good Clinical Practice: Integrated Addendum to ICH E6(R1): Guidance for Industry March 2018
USA FDA INFORMATION SHEET - Recruiting Study Subjects, Guidance for Institutional Review Boards and Clinical Investigators Jan-1998 -HM-ENUSA FDA INFORMATION SHEET - Recruiting Study Subjects, Guidance for Institutional Review Boards and Clinical Investigators Jan-1998
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