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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.
F
FRA AEC DOC012 v03 Avis aux promoteurs d’investigations cliniques de DM (RIPH1) – Partie II 16-May-2025 2.-002 +
TAG-00321-Age-pro ++ TAG-00046-Ser-sSc ++ TAG-00279-Hea-rFr ++ TAG-00155-Med-Med ++ TAG-00134-Eth-kom  +
FRA Code de la Santé Publique - Partie législative - 1ere partie, Livre 1er, Titre II 16-May-2025 L5311-1 +
TAG-00321-Age-pro ++ TAG-00057-Com-deR ++ TAG-00177-Ben-koB  +
FRA AEC DOC010 V.04 01-Jun-2018 - +
TAG-00321-Age-pro ++ TAG-00059-Reg-lat ++ TAG-00264-Eud-lin ++ TAG-00008-Cli-ngK ++ TAG-00001-Med-rzn  +
FRA AEC-DM-DMDIV DOC006 v04 AAP RDM Partie II Modalités pratiques 16-May-2025 - +
TAG-00321-Age-pro ++ TAG-00155-Med-Med ++ TAG-00059-Reg-lat  +
I
ICH ICH E6 Guideline R3 (2025) Appendix B 2.5 +
TAG-00328-Com-egu ++ TAG-00033-Pro-oto ++ TAG-00043-Goo-tek ++ TAG-00041-Ame-run  +
G
GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Schedule 1 Part 2 6. +
TAG-00328-Com-egu ++ TAG-00033-Pro-oto ++ TAG-00043-Goo-tek ++ TAG-00134-Eth-kom  +
I
ICH ICH E6 Guideline R3 (2025) III. Annex 1 2.5 +
TAG-00328-Com-egu ++ TAG-00033-Pro-oto ++ TAG-00246-Inv-hte ++ TAG-00043-Goo-tek ++ TAG-00111-Agr-chr  +
ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 10.6 +
TAG-00328-Com-egu ++ TAG-00203-Cli-lin ++ TAG-00019-Pri-Prü ++ TAG-00150-Sou-eUr ++ TAG-00246-Inv-hte  +
W
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 4.4 - Introduction +
TAG-00328-Com-egu ++ TAG-00203-Cli-lin ++ TAG-00246-Inv-hte ++ TAG-00111-Agr-chr  +
I
ICH ICH E6 Guideline R3 (2025) GLOSSARY - Compliance (in relation to trials) +
TAG-00328-Com-egu ++ TAG-00244-Def-ini ++ TAG-00340-Req-nfo ++ TAG-00043-Goo-tek  +
U
USA 21 CFR Part 812 09-Apr-2025 § 812.46 (a) +
TAG-00328-Com-egu ++ TAG-00245-Spo-ten ++ TAG-00137-Mon-che ++ TAG-00143-Non-abw ++ TAG-00320-Foo-eri  +
USA 21 CFR Part 812 09-Apr-2025 § 812.110 (b) +
TAG-00328-Com-egu ++ TAG-00246-Inv-hte ++ TAG-00111-Agr-chr ++ TAG-00155-Med-Med ++ TAG-00320-Foo-eri  +
I
ICH ICH E6 Guideline R3 (2025) III. Annex 1 3.13.1 +
TAG-00329-Saf-lne ++ TAG-00017-Spo-die ++ TAG-00045-Adv-hte ++ TAG-00082-Scr-hlu  +
ICH ICH E6 Guideline R3 (2025) III. Annex 1 2.7.2 (a) - (d) +
TAG-00329-Saf-lne ++ TAG-00045-Adv-hte ++ TAG-00250-Inv-sme ++ TAG-00017-Spo-die ++ TAG-00033-Pro-oto  +
ICH ICH E2A Guideline 1994 III A. 2. +
TAG-00329-Saf-lne ++ TAG-00046-Ser-sSc ++ TAG-00252-Exp-hle ++ TAG-00327-Exa-spi  +
ICH ICH E6 Guideline R3 (2025) III. Annex 1 2.7.2 (a) +
TAG-00329-Saf-lne ++ TAG-00082-Scr-hlu ++ TAG-00045-Adv-hte ++ TAG-00250-Inv-sme  +
E
EU Recommendations of the expert group - Risk proportionate approaches in clinical trials 25-Apr-2017 2. +
TAG-00329-Saf-lne ++ TAG-00176-Ris-erh ++ TAG-00011-Inv-tud ++ TAG-00055-Stu-ngs ++ TAG-00009-Low-gra ++ TAG-00032-Inf-ngs  +
G
GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 2 unexpected adverse reaction +
TAG-00331-Une-irk ++ TAG-00003-Adv-cht ++ TAG-00244-Def-ini ++ TAG-00067-Exp-war  +
GBR Directive 2001/20/EC 04-Apr-2001 Article 2 (p) +
TAG-00331-Une-irk ++ TAG-00003-Adv-cht ++ TAG-00244-Def-ini ++ TAG-00034-Inv-Bro ++ TAG-00067-Exp-war  +
I
ICH ICH E2A Guideline 1994 II A. 3. +
TAG-00331-Une-irk ++ TAG-00003-Adv-cht ++ TAG-00244-Def-ini ++ TAG-00034-Inv-Bro  +
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