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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
ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 Annex B +
TAG-00034-Inv-Bro  +
U
USA 21 CFR Part 312 09-Apr-2025 § 312.23 (a) ; (5) +
TAG-00034-Inv-Bro ++ TAG-00011-Inv-tud ++ TAG-00320-Foo-eri ++ TAG-00017-Spo-die  +
I
ICH ICH E6 Guideline R3 (2025) Appendix A 3.4 +
TAG-00034-Inv-Bro ++ TAG-00011-Inv-tud ++ TAG-00095-Sto-ung ++ TAG-00035-Man-odu  +
W
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - investigator’s brochure +
TAG-00034-Inv-Bro ++ TAG-00244-Def-ini  +
I
ICH ICH E6 Guideline R3 (2025) GLOSSARY - Investigator’s Brochure (IB) +
TAG-00034-Inv-Bro ++ TAG-00244-Def-ini ++ TAG-00204-Cli-tbe  +
ICH ICH E6 Guideline R3 (2025) Appendix A +
TAG-00034-Inv-Bro ++ TAG-00340-Req-nfo  +
G
GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Schedule 7 Part 2 2. +
TAG-00035-Man-odu ++ TAG-00011-Inv-tud ++ TAG-00132-Goo-rst ++ TAG-00057-Com-deR  +
D
DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 31 +
TAG-00036-Sta-ung ++ TAG-00201-Cli-eSt ++ TAG-00053-Dev-las ++ TAG-00134-Eth-kom ++ TAG-00155-Med-Med  +
DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 31a +
TAG-00036-Sta-ung ++ TAG-00231-Per-ung ++ TAG-00176-Ris-erh ++ TAG-00220-Inv-agn  +
E
EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 2 Paragraph 26 - 29 +
TAG-00037-End-ung ++ TAG-00038-Ear-tig ++ TAG-00244-Def-ini ++ TAG-00087-End-Pat  +
EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 37 Paragraph 1 – 7 +
TAG-00037-End-ung ++ TAG-00039-Tem-ung ++ TAG-00038-Ear-tig ++ TAG-00262-CTI-Kli ++ TAG-00017-Spo-die  +
G
GBR The Medical Devices Regulations 2002 11-Feb-2021 Article 16 (11) +
TAG-00037-End-ung ++ TAG-00088-Clo-esu ++ TAG-00201-Cli-eSt ++ TAG-00181-Man-npr ++ TAG-00155-Med-Med  +
E
EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 77 Paragraph 4 – 5 +
TAG-00037-End-ung ++ TAG-00201-Cli-eSt ++ TAG-00017-Spo-die ++ TAG-00142-Mul-ent ++ TAG-00253-Rep-att  +
G
GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 27 +
TAG-00037-End-ung ++ TAG-00253-Rep-att ++ TAG-00017-Spo-die ++ TAG-00134-Eth-kom ++ TAG-00057-Com-deR  +
GBR Directive 2001/20/EC 04-Apr-2001 Article 10 (c) +
TAG-00037-End-ung ++ TAG-00253-Rep-att ++ TAG-00017-Spo-die ++ TAG-00134-Eth-kom ++ TAG-00057-Com-deR  +
E
EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 37 Paragraph 4 +
TAG-00037-End-ung ++ TAG-00274-Fin-Spo ++ TAG-00275-Lay-ndl ++ TAG-00264-Eud-lin ++ TAG-00017-Spo-die  +
G
GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Schedule 3 Part 1 1. (p) +
TAG-00037-End-ung ++ TAG-00287-Sto-pre ++ TAG-00134-Eth-kom ++ TAG-00343-Doc-ten ++ TAG-00033-Pro-oto  +
I
ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 8.2 +
TAG-00038-Ear-tig ++ TAG-00039-Tem-ung ++ TAG-00201-Cli-eSt ++ TAG-00017-Spo-die ++ TAG-00133-Ind-rhe  +
ICH ICH E6 Guideline R3 (2025) III. Annex 1 2.6 +
TAG-00038-Ear-tig ++ TAG-00039-Tem-ung ++ TAG-00246-Inv-hte ++ TAG-00025-Sub-mer  +
E
EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 38 +
TAG-00038-Ear-tig ++ TAG-00039-Tem-ung ++ TAG-00329-Saf-lne ++ TAG-00177-Ben-koB ++ TAG-00262-CTI-Kli  +
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