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Property:RefTags

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Raw TAG-ID list for this reference (used for glossary queries).

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Showing 20 pages using this property.
U
USA 45 CFR Part 46 09-Apr-2025 § 46.124 +
TAG-00134-Eth-kom ++ TAG-00340-Req-nfo  +
USA 21 CFR Part 56 09-Apr-2025 § 56.109 +
TAG-00134-Eth-kom ++ TAG-00340-Req-nfo ++ TAG-00018-Inv-die  +
USA 21 CFR Part 56 09-Apr-2025 Subpart C +
TAG-00134-Eth-kom ++ TAG-00340-Req-nfo ++ TAG-00052-Ris-ein  +
USA 45 CFR Part 46 09-Apr-2025 § 46.107 - § 46.112 +
TAG-00134-Eth-kom ++ TAG-00340-Req-nfo ++ TAG-00052-Ris-ein  +
USA 45 CFR Part 46 09-Apr-2025 Subpart E +
TAG-00134-Eth-kom ++ TAG-00340-Req-nfo ++ TAG-00328-Com-egu  +
USA 21 CFR Part 56 09-Apr-2025 § 56.103 +
TAG-00134-Eth-kom ++ TAG-00340-Req-nfo ++ TAG-00320-Foo-eri ++ TAG-00201-Cli-eSt  +
I
ICH ICH E6 Guideline R3 (2025) III. Annex 1 1 +
TAG-00134-Eth-kom ++ TAG-00341-Res-ben ++ TAG-00340-Req-nfo  +
W
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 3.2 - Introduction +
TAG-00134-Eth-kom ++ TAG-00341-Res-ben ++ TAG-00051-Eth-ngs ++ TAG-00329-Saf-lne  +
U
USA 21 CFR Part 812 09-Apr-2025 Subpart D +
TAG-00134-Eth-kom ++ TAG-00341-Res-ben ++ TAG-00155-Med-Med ++ TAG-00320-Foo-eri  +
USA 45 CFR Part 46 09-Apr-2025 § 46.115 +
TAG-00134-Eth-kom ++ TAG-00343-Doc-ten ++ TAG-00340-Req-nfo  +
E
EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 50 +
TAG-00135-Inv-ntr ++ TAG-00342-Sit-der ++ TAG-00340-Req-nfo  +
I
ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 10.3 +
TAG-00135-Inv-ntr ++ TAG-00342-Sit-der ++ TAG-00019-Pri-Prü ++ TAG-00083-Enr-enr ++ TAG-00201-Cli-eSt  +
ICH ICH E6 Guideline R3 (2025) GLOSSARY - Metadata +
TAG-00136-Met-ate ++ TAG-00244-Def-ini  +
ICH ICH E6 Guideline R3 (2025) III. Annex 1 3.11.4.5.3 +
TAG-00137-Mon-che ++ TAG-00095-Sto-ung ++ TAG-00093-Dru-ent ++ TAG-00097-Exp-dat ++ TAG-00011-Inv-tud  +
W
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 4.12-001 +
TAG-00137-Mon-che ++ TAG-00113-Aud-tQu ++ TAG-00044-Ins-ion ++ TAG-00246-Inv-hte  +
E
EU EMA/INS/GCP/126568/2023 - Annual Report of the Good Clinical Practice (GCP) Inspectors' Working Group (IWG) 2022 2023 3.1.2 - Monitoring +
TAG-00137-Mon-che ++ TAG-00138-Rem-oni ++ TAG-00118-Cri-rit ++ TAG-00119-Maj-heF ++ TAG-00327-Exa-spi  +
I
ICH ICH E6 Guideline R3 (2025) III. Annex 1 3.11.4 3.11.4.1 - 3.11.4.2 +
TAG-00137-Mon-che ++ TAG-00138-Rem-oni ++ TAG-00293-Cen-sMo ++ TAG-00017-Spo-die ++ TAG-00139-Mon-lan  +
ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 9.2.4 +
TAG-00137-Mon-che ++ TAG-00139-Mon-lan ++ TAG-00201-Cli-eSt ++ TAG-00329-Saf-lne ++ TAG-00317-Obj-set  +
E
EU Recommendations of the expert group - Risk proportionate approaches in clinical trials 25-Apr-2017 4.4 +
TAG-00137-Mon-che ++ TAG-00140-Ris-nRi ++ TAG-00129-Dat-ali ++ TAG-00317-Obj-set  +
U
USA FDA Guidance for Industry - Oversight of Clinical Investigations — A Risk-Based Approach to Monitoring Aug-2013 IV A. Verification +
TAG-00137-Mon-che ++ TAG-00140-Ris-nRi ++ TAG-00029-Inf-rte ++ TAG-00065-Sou-nüb  +
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