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Property:RefTags

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Text

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

previous 202050100250500next 20
Showing 20 pages using this property.
I
ICH ICH E6 Guideline R3 (2025) III. Annex 1 3.17.1 +
TAG-00038-Ear-tig ++ TAG-00039-Tem-ung ++ TAG-00245-Spo-ten ++ TAG-00057-Com-deR  +
E
EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 77 Paragraph 1 – 3 +
TAG-00038-Ear-tig ++ TAG-00039-Tem-ung ++ TAG-00201-Cli-eSt ++ TAG-00017-Spo-die ++ TAG-00329-Saf-lne  +
U
USA 21 CFR Part 312 09-Apr-2025 § 312.56 +
TAG-00038-Ear-tig ++ TAG-00176-Ris-erh ++ TAG-00017-Spo-die ++ TAG-00134-Eth-kom ++ TAG-00320-Foo-eri  +
G
GBR Directive 93/42/EEC 11-Oct-2007 Article 15 6. - 7.-001 +
TAG-00038-Ear-tig ++ TAG-00201-Cli-eSt ++ TAG-00329-Saf-lne ++ TAG-00214-Ser-hei ++ TAG-00057-Com-deR  +
U
USA 21 CFR Part 812 09-Apr-2025 § 812.3 (q) +
TAG-00038-Ear-tig ++ TAG-00244-Def-ini ++ TAG-00155-Med-Med ++ TAG-00320-Foo-eri  +
W
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 5.14 +
TAG-00038-Ear-tig ++ TAG-00245-Spo-ten ++ TAG-00134-Eth-kom ++ TAG-00057-Com-deR  +
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 4.15 +
TAG-00038-Ear-tig ++ TAG-00246-Inv-hte ++ TAG-00057-Com-deR ++ TAG-00134-Eth-kom  +
U
USA 21 CFR Part 312 09-Apr-2025 § 312.44 +
TAG-00038-Ear-tig ++ TAG-00268-Wit-DIN ++ TAG-00011-Inv-tud ++ TAG-00017-Spo-die ++ TAG-00320-Foo-eri  +
USA 21 CFR Part 312 09-Apr-2025 § 312.44 (d) +
TAG-00038-Ear-tig ++ TAG-00268-Wit-DIN ++ TAG-00011-Inv-tud ++ TAG-00320-Foo-eri  +
USA 45 CFR Part 46 09-Apr-2025 § 46.123 +
TAG-00038-Ear-tig ++ TAG-00340-Req-nfo  +
USA 21 CFR Part 312 09-Apr-2025 § 312.45 +
TAG-00039-Tem-ung ++ TAG-00011-Inv-tud ++ TAG-00320-Foo-eri ++ TAG-00017-Spo-die  +
E
EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 77 Paragraph 1, 3 & 4 +
TAG-00039-Tem-ung ++ TAG-00038-Ear-tig ++ TAG-00037-End-ung ++ TAG-00201-Cli-eSt ++ TAG-00017-Spo-die  +
EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 77 +
TAG-00039-Tem-ung ++ TAG-00038-Ear-tig ++ TAG-00201-Cli-eSt ++ TAG-00017-Spo-die ++ TAG-00329-Saf-lne  +
EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 73 Paragraph 1, 3, 4 +
TAG-00039-Tem-ung ++ TAG-00038-Ear-tig ++ TAG-00231-Per-ung ++ TAG-00017-Spo-die  +
G
GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 31 +
TAG-00039-Tem-ung ++ TAG-00038-Ear-tig ++ TAG-00057-Com-deR ++ TAG-00329-Saf-lne ++ TAG-00008-Cli-ngK  +
U
USA 21 CFR Part 312 09-Apr-2025 § 312.42 +
TAG-00039-Tem-ung ++ TAG-00329-Saf-lne ++ TAG-00011-Inv-tud ++ TAG-00320-Foo-eri ++ TAG-00017-Spo-die  +
G
GBR Directive 2001/20/EC 04-Apr-2001 Article 10 (b)-001 +
TAG-00039-Tem-ung ++ TAG-00329-Saf-lne ++ TAG-00057-Com-deR ++ TAG-00069-Imm-rhe ++ TAG-00011-Inv-tud  +
GBR Directive 2001/20/EC 04-Apr-2001 Article 10 (b)-002 +
TAG-00039-Tem-ung ++ TAG-00329-Saf-lne ++ TAG-00069-Imm-rhe ++ TAG-00011-Inv-tud ++ TAG-00057-Com-deR  +
D
DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 63 g Absatz 3 +
TAG-00040-Sub-Änd ++ TAG-00041-Ame-run ++ TAG-00033-Pro-oto ++ TAG-00057-Com-deR  +
DEU KPBV - Klinische Prüfung-Bewertungsverfahren-Verordnung 31-Jan-2022 § 9 +
TAG-00040-Sub-Änd ++ TAG-00041-Ame-run ++ TAG-00134-Eth-kom ++ TAG-00008-Cli-ngK ++ TAG-00057-Com-deR  +
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