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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.
E
EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 75 +
TAG-00040-Sub-Änd ++ TAG-00201-Cli-eSt ++ TAG-00017-Spo-die ++ TAG-00329-Saf-lne ++ TAG-00155-Med-Med  +
EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 71 +
TAG-00040-Sub-Änd ++ TAG-00231-Per-ung ++ TAG-00017-Spo-die ++ TAG-00329-Saf-lne ++ TAG-00220-Inv-agn  +
EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 2 Paragraph 13 +
TAG-00040-Sub-Änd ++ TAG-00244-Def-ini ++ TAG-00329-Saf-lne ++ TAG-00008-Cli-ngK  +
D
DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 63g (3) +
TAG-00040-Sub-Änd ++ TAG-00285-Pha-enk ++ TAG-00033-Pro-oto ++ TAG-00057-Com-deR ++ TAG-00276-Mar-inh  +
DEU Gemeinsame Empfehlungen - zur Anzeige von Anwendungsbeobachtungen und nichtinterventionellen Unbedenklichkeits-studien 15-Dec-2022 2.4 +
TAG-00041-Ame-run ++ TAG-00010-Non-Stu ++ TAG-00057-Com-deR  +
DEU DGEPi - GEP Guter Epidemiologischer Praxis Sep-2018 Leitlinie 6 6.3 +
TAG-00041-Ame-run ++ TAG-00010-Non-Stu ++ TAG-00144-Qua-gew ++ TAG-00343-Doc-ten  +
U
USA 21 CFR Part 312 09-Apr-2025 § 312.31 +
TAG-00041-Ame-run ++ TAG-00017-Spo-die ++ TAG-00011-Inv-tud ++ TAG-00340-Req-nfo ++ TAG-00320-Foo-eri  +
W
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 4.4 - Amendment +
TAG-00041-Ame-run ++ TAG-00017-Spo-die ++ TAG-00246-Inv-hte ++ TAG-00329-Saf-lne ++ TAG-00033-Pro-oto  +
G
GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 22-23 +
TAG-00041-Ame-run ++ TAG-00017-Spo-die ++ TAG-00057-Com-deR ++ TAG-00008-Cli-ngK  +
U
USA 21 CFR Part 312 09-Apr-2025 § 312.30 +
TAG-00041-Ame-run ++ TAG-00033-Pro-oto ++ TAG-00011-Inv-tud ++ TAG-00018-Inv-die ++ TAG-00320-Foo-eri  +
I
ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 7.5.1 +
TAG-00041-Ame-run ++ TAG-00034-Inv-Bro ++ TAG-00203-Cli-lin ++ TAG-00030-Inf-onu ++ TAG-00201-Cli-eSt  +
U
USA 21 CFR Part 312 09-Apr-2025 § 312.30 (b) (ii) +
TAG-00041-Ame-run ++ TAG-00069-Imm-rhe ++ TAG-00011-Inv-tud ++ TAG-00320-Foo-eri ++ TAG-00033-Pro-oto  +
W
WMA Declaration of Helsinki 2024 Paragraph 23 - Amendment approval +
TAG-00041-Ame-run ++ TAG-00134-Eth-kom ++ TAG-00033-Pro-oto ++ TAG-00051-Eth-ngs  +
G
GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 25 +
TAG-00041-Ame-run ++ TAG-00134-Eth-kom ++ TAG-00033-Pro-oto ++ TAG-00017-Spo-die ++ TAG-00057-Com-deR  +
U
USA 21 CFR Part 56 09-Apr-2025 § 56.110 (b) (2) +
TAG-00041-Ame-run ++ TAG-00134-Eth-kom ++ TAG-00052-Ris-ein ++ TAG-00320-Foo-eri  +
D
DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 54 +
TAG-00041-Ame-run ++ TAG-00201-Cli-eSt ++ TAG-00057-Com-deR ++ TAG-00134-Eth-kom ++ TAG-00017-Spo-die  +
I
ICH ICH E6 Guideline R3 (2025) GLOSSARY - Protocol Amendment +
TAG-00041-Ame-run ++ TAG-00244-Def-ini ++ TAG-00033-Pro-oto  +
G
GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 11 +
TAG-00041-Ame-run ++ TAG-00244-Def-ini ++ TAG-00033-Pro-oto ++ TAG-00134-Eth-kom ++ TAG-00008-Cli-ngK  +
GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 24 +
TAG-00042-Non-ügi ++ TAG-00041-Ame-run ++ TAG-00017-Spo-die ++ TAG-00134-Eth-kom  +
GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 28 +
TAG-00043-Goo-tek ++ TAG-00025-Sub-mer ++ TAG-00017-Spo-die ++ TAG-00008-Cli-ngK  +
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