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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.
I
ICH ICH E6 Guideline - Annex 2 R3 Annex 2 Annex 2 2.2 +
TAG-00029-Inf-rte ++ TAG-00032-Inf-ngs ++ TAG-00028-Leg-ich ++ TAG-00246-Inv-hte ++ TAG-00294-Rem-gFe  +
D
DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 96 Nr. 10, 11, 21 +
TAG-00029-Inf-rte ++ TAG-00049-Ser-Ver ++ TAG-00201-Cli-eSt ++ TAG-00001-Med-rzn  +
E
EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 63 Paragraph 6 – 7 +
TAG-00029-Inf-rte ++ TAG-00050-Cli-ber ++ TAG-00263-EUD-izi ++ TAG-00201-Cli-eSt ++ TAG-00155-Med-Med  +
EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 59 Paragraph 6 – 7 +
TAG-00029-Inf-rte ++ TAG-00050-Cli-ber ++ TAG-00263-EUD-izi ++ TAG-00231-Per-ung  +
W
WMA Declaration of Helsinki 2024 Paragraph 25 – 28 +
TAG-00029-Inf-rte ++ TAG-00051-Eth-ngs ++ TAG-00025-Sub-mer  +
D
DEU DGEPi - GEP Guter Epidemiologischer Praxis Sep-2018 Leitlinie 1 1.2 +
TAG-00029-Inf-rte ++ TAG-00051-Eth-ngs ++ TAG-00010-Non-Stu ++ TAG-00025-Sub-mer  +
U
USA 21 CFR Part 50 09-Apr-2025 § 50.22 +
TAG-00029-Inf-rte ++ TAG-00052-Ris-ein ++ TAG-00134-Eth-kom ++ TAG-00201-Cli-eSt ++ TAG-00320-Foo-eri  +
E
EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 28 Paragraph 2-3 +
TAG-00029-Inf-rte ++ TAG-00063-Dat-per ++ TAG-00017-Spo-die ++ TAG-00028-Leg-ich  +
U
USA 21 CFR Part 50 09-Apr-2025 § 50.23 +
TAG-00029-Inf-rte ++ TAG-00069-Imm-rhe ++ TAG-00320-Foo-eri ++ TAG-00201-Cli-eSt  +
USA 21 CFR Part 50 09-Apr-2025 § 50.24 +
TAG-00029-Inf-rte ++ TAG-00069-Imm-rhe ++ TAG-00340-Req-nfo ++ TAG-00320-Foo-eri  +
W
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 3.3 c) ; e) - g) +
TAG-00029-Inf-rte ++ TAG-00072-Ins-her ++ TAG-00025-Sub-mer ++ TAG-00031-Pat-onA  +
E
EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 34 +
TAG-00029-Inf-rte ++ TAG-00154-Vul-eil ++ TAG-00008-Cli-ngK  +
EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 2 Paragraph 58 +
TAG-00029-Inf-rte ++ TAG-00244-Def-ini ++ TAG-00231-Per-ung ++ TAG-00026-Min-isc ++ TAG-00027-Inc-son ++ TAG-00028-Leg-ich  +
W
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - informed consent +
TAG-00029-Inf-rte ++ TAG-00244-Def-ini ++ TAG-00043-Goo-tek ++ TAG-00343-Doc-ten  +
U
USA Informed Consent - FDA Guidance for IRBs, Clinical Investigators, and Sponsors Aug-2023 IV. +
TAG-00029-Inf-rte ++ TAG-00246-Inv-hte ++ TAG-00329-Saf-lne ++ TAG-00320-Foo-eri  +
E
EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 29 Paragraph 6-8 +
TAG-00029-Inf-rte ++ TAG-00275-Lay-ndl ++ TAG-00264-Eud-lin ++ TAG-00025-Sub-mer  +
EU EMA/INS/GCP/112288/2023 - Guideline on computerised systems and electronic data in clinical trials 2023 Annex A A5.3 +
TAG-00029-Inf-rte ++ TAG-00286-Ele-sch ++ TAG-00134-Eth-kom ++ TAG-00032-Inf-ngs ++ TAG-00043-Goo-tek  +
U
USA 21 CFR Part 50 09-Apr-2025 § 50.20 +
TAG-00029-Inf-rte ++ TAG-00320-Foo-eri ++ TAG-00340-Req-nfo ++ TAG-00018-Inv-die  +
I
ICH ICH E6 Guideline R3 (2025) III. Annex 1 2.8 +
TAG-00029-Inf-rte ++ TAG-00340-Req-nfo ++ TAG-00025-Sub-mer  +
D
DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 28 Absatz 1 – 2 +
TAG-00029-Inf-rte ++ TAG-00340-Req-nfo ++ TAG-00025-Sub-mer ++ TAG-00155-Med-Med  +
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