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Property:RefTags

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

previous 202050100250500next 20
Showing 20 pages using this property.
U
USA 21 CFR Part 312 09-Apr-2025 § 312.69 +
TAG-00095-Sto-ung ++ TAG-00011-Inv-tud ++ TAG-00246-Inv-hte  +
E
EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 ANNEX VI Section D No. 8 +
TAG-00098-IMP-tik ++ TAG-00123-Bli-ppe ++ TAG-00307-Int-gsu ++ TAG-00167-Lab-ttP  +
EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 69 +
TAG-00098-IMP-tik ++ TAG-00167-Lab-ttP ++ TAG-00340-Req-nfo ++ TAG-00011-Inv-tud  +
D
DEU DGEPi - GEP Guter Epidemiologischer Praxis Sep-2018 Leitlinie 5 +
TAG-00109-Bio-osi ++ TAG-00029-Inf-rte ++ TAG-00010-Non-Stu ++ TAG-00104-Bio-sch  +
DEU DGEPi - GEP Guter Epidemiologischer Praxis Sep-2018 Leitlinie 9 +
TAG-00111-Agr-chr ++ TAG-00010-Non-Stu ++ TAG-00017-Spo-die  +
I
ICH ICH E6 Guideline R3 (2025) III. Annex 1 3.5 +
TAG-00111-Agr-chr ++ TAG-00017-Spo-die ++ TAG-00343-Doc-ten ++ TAG-00018-Inv-die  +
W
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 4.11 +
TAG-00111-Agr-chr ++ TAG-00017-Spo-die ++ TAG-00033-Pro-oto ++ TAG-00018-Inv-die  +
I
ICH ICH E6 Guideline R3 (2025) III. Annex 1 3.6 +
TAG-00111-Agr-chr ++ TAG-00017-Spo-die ++ TAG-00147-Ser-inD ++ TAG-00133-Ind-rhe ++ TAG-00340-Req-nfo  +
ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 6.9 +
TAG-00111-Agr-chr ++ TAG-00061-Cli-rtr ++ TAG-00019-Pri-Prü ++ TAG-00201-Cli-eSt ++ TAG-00148-Con-rsc  +
W
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - contract +
TAG-00111-Agr-chr ++ TAG-00244-Def-ini ++ TAG-00017-Spo-die ++ TAG-00060-Del-ben  +
I
ICH ICH E6 Guideline R3 (2025) GLOSSARY - Agreement +
TAG-00111-Agr-chr ++ TAG-00244-Def-ini ++ TAG-00060-Del-ben ++ TAG-00033-Pro-oto  +
F
FRA Code de la Santé Publique - Partie Réglementaire - 1ere partie, Livre 1er, Titre II 16-May-2025 Article R1121-3-1 +
TAG-00111-Agr-chr ++ TAG-00340-Req-nfo ++ TAG-00191-Hea-ken ++ TAG-00017-Spo-die  +
I
ICH ICH E6 Guideline R3 (2025) III. Annex 1 1.2.7 +
TAG-00112-Ass-nve ++ TAG-00026-Min-isc ++ TAG-00134-Eth-kom ++ TAG-00340-Req-nfo  +
ICH ICH E6 Guideline R3 (2025) III. Annex 1 2.8.12 +
TAG-00112-Ass-nve ++ TAG-00026-Min-isc ++ TAG-00032-Inf-ngs ++ TAG-00029-Inf-rte  +
U
USA 21 CFR Part 50 09-Apr-2025 § 50.3 (n) +
TAG-00112-Ass-nve ++ TAG-00244-Def-ini ++ TAG-00026-Min-isc  +
W
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 4.12-002 +
TAG-00113-Aud-tQu ++ TAG-00044-Ins-ion ++ TAG-00137-Mon-che ++ TAG-00246-Inv-hte  +
I
ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 7.11 +
TAG-00113-Aud-tQu ++ TAG-00044-Ins-ion ++ TAG-00317-Obj-set ++ TAG-00135-Inv-ntr  +
ICH ICH E6 Guideline R3 (2025) III. Annex 1 3.11.2 +
TAG-00113-Aud-tQu ++ TAG-00144-Qua-gew ++ TAG-00291-Qua-tsk ++ TAG-00343-Doc-ten ++ TAG-00017-Spo-die  +
IMDRF IMDRF – Guidelines - - +
TAG-00113-Aud-tQu ++ TAG-00155-Med-Med ++ TAG-00218-Har-päi  +
ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 Annex J +
TAG-00113-Aud-tQu ++ TAG-00201-Cli-eSt  +
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