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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.
E
EU GVP: Module VIII EMA/813938/2011 Rev. 3 (2017) VIII.B.5 +
TAG-00075-Pub-ich ++ TAG-00285-Pha-enk ++ TAG-00276-Mar-inh ++ TAG-00019-Pri-Prü ++ TAG-00111-Agr-chr  +
D
DEU DGEPi - GEP Guter Epidemiologischer Praxis Sep-2018 Leitlinie 10 +
TAG-00075-Pub-ich ++ TAG-00338-Met-odi ++ TAG-00010-Non-Stu ++ TAG-00341-Res-ben  +
DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 42b +
TAG-00075-Pub-ich ++ TAG-00340-Req-nfo ++ TAG-00017-Spo-die ++ TAG-00057-Com-deR ++ TAG-00001-Med-rzn  +
I
ICH ICH E8 Guideline R1 (2021) 3.3.5 +
TAG-00076-Fea-ung ++ TAG-00055-Stu-ngs ++ TAG-00033-Pro-oto ++ TAG-00144-Qua-gew  +
ICH ICH E8 Guideline R1 (2021) 7 +
TAG-00077-Inc-gsk ++ TAG-00033-Pro-oto ++ TAG-00317-Obj-set  +
ICH ICH E8 Guideline R1 (2021) 5.1 +
TAG-00077-Inc-gsk ++ TAG-00078-Exc-ssk ++ TAG-00317-Obj-set ++ TAG-00083-Enr-enr ++ TAG-00244-Def-ini  +
G
GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Schedule 3 Part 1 1. (i) +
TAG-00077-Inc-gsk ++ TAG-00078-Exc-ssk ++ TAG-00154-Vul-eil ++ TAG-00134-Eth-kom ++ TAG-00343-Doc-ten  +
U
USA 21 CFR Part 312 09-Apr-2025 § 312.23 (6) (c) - (d) +
TAG-00077-Inc-gsk ++ TAG-00078-Exc-ssk ++ TAG-00033-Pro-oto ++ TAG-00320-Foo-eri ++ TAG-00011-Inv-tud  +
I
ICH ICH E6 Guideline R3 (2025) Appendix B 5 +
TAG-00077-Inc-gsk ++ TAG-00078-Exc-ssk ++ TAG-00079-Pre-eni ++ TAG-00082-Scr-hlu ++ TAG-00033-Pro-oto  +
E
EU EMA/298712/2022 - Complex clinical trials – Questions and answers 23-May-2022 Q5.2 +
TAG-00079-Pre-eni ++ TAG-00082-Scr-hlu ++ TAG-00083-Enr-enr ++ TAG-00033-Pro-oto  +
EU EMA/786433/2022 Annex V – to guidance for the conduct of good clinical practice inspections – Phase I units 15-Nov-2022 2.9 +
TAG-00083-Enr-enr ++ TAG-00029-Inf-rte ++ TAG-00082-Scr-hlu ++ TAG-00281-Und-sse  +
EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 ANNEX I Section K No. 59-60 +
TAG-00083-Enr-enr ++ TAG-00033-Pro-oto ++ TAG-00343-Doc-ten  +
I
ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 3.42 - recruitment +
TAG-00083-Enr-enr ++ TAG-00244-Def-ini ++ TAG-00201-Cli-eSt  +
W
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 4.3 +
TAG-00083-Enr-enr ++ TAG-00246-Inv-hte ++ TAG-00033-Pro-oto ++ TAG-00025-Sub-mer  +
D
DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 33 Absatz 2 +
TAG-00083-Enr-enr ++ TAG-00343-Doc-ten ++ TAG-00031-Pat-onA ++ TAG-00033-Pro-oto  +
I
ICH ICH E6 Guideline R3 (2025) Appendix B 9.4 +
TAG-00086-Fol-Fol ++ TAG-00045-Adv-hte ++ TAG-00071-Pre-nis ++ TAG-00025-Sub-mer  +
ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 8.3 +
TAG-00088-Clo-esu ++ TAG-00131-Ess-sun ++ TAG-00073-Arc-arc ++ TAG-00201-Cli-eSt ++ TAG-00019-Pri-Prü  +
ICH ICH E6 Guideline R3 (2025) III. Annex 1 3.11.4.5.2 +
TAG-00088-Clo-esu ++ TAG-00131-Ess-sun ++ TAG-00093-Dru-ent ++ TAG-00135-Inv-ntr  +
U
USA 21 CFR Part 812 09-Apr-2025 § 812.140 (a) (2) +
TAG-00093-Dru-ent ++ TAG-00202-Inv-Pro ++ TAG-00343-Doc-ten ++ TAG-00155-Med-Med ++ TAG-00246-Inv-hte  +
USA 21 CFR Part 312 09-Apr-2025 § 312.62 (a) +
TAG-00093-Dru-ent ++ TAG-00272-Ret-enA ++ TAG-00343-Doc-ten ++ TAG-00246-Inv-hte  +
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