Personal tools

Sponsorname

Your company could advertise here

www.fla-consulting.eu

Property:RefTags

From GxPlex

Jump to: navigation, search

Text

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

previous 202050100250500next 20
Showing 20 pages using this property.
U
USA NIH - SCORE Manual: Appendix Source Documents Requirements Rev 01 16-Aug-2025 Page 3 - Note +
TAG-00124-Cas-Prü ++ TAG-00150-Sou-eUr ++ TAG-00064-Ele-eUn ++ TAG-00033-Pro-oto  +
I
ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 6.6 +
TAG-00124-Cas-Prü ++ TAG-00203-Cli-lin ++ TAG-00201-Cli-eSt ++ TAG-00155-Med-Med  +
W
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - case -report form (CRF) +
TAG-00124-Cas-Prü ++ TAG-00244-Def-ini ++ TAG-00033-Pro-oto  +
I
ICH ICH E6 Guideline R3 (2025) GLOSSARY - Case Report Form (CRF) +
TAG-00124-Cas-Prü ++ TAG-00244-Def-ini ++ TAG-00128-Dat-rkz ++ TAG-00017-Spo-die  +
U
USA 21 CFR Part 812 09-Apr-2025 § 812.140 (a) (3) +
TAG-00124-Cas-Prü ++ TAG-00272-Ret-enA ++ TAG-00155-Med-Med ++ TAG-00320-Foo-eri ++ TAG-00246-Inv-hte  +
USA 21 CFR Part 312 09-Apr-2025 § 312.62 (b) +
TAG-00124-Cas-Prü ++ TAG-00272-Ret-enA ++ TAG-00343-Doc-ten ++ TAG-00320-Foo-eri ++ TAG-00246-Inv-hte  +
D
DEU DGEPi - GEP Guter Epidemiologischer Praxis Sep-2018 Leitlinie 6 6.8 +
TAG-00125-Ele-ekt ++ TAG-00144-Qua-gew ++ TAG-00010-Non-Stu ++ TAG-00124-Cas-Prü  +
U
USA FDA Guidance for Industry - Electronic Source Data in Clinical Investigations Sep-2013 GLOSSARY OF TERMS +
TAG-00126-Cer-rte ++ TAG-00244-Def-ini ++ TAG-00149-Sig-nds ++ TAG-00324-Med-Age  +
I
ICH ICH E6 Guideline R3 (2025) GLOSSARY - Certified Copy +
TAG-00126-Cer-rte ++ TAG-00244-Def-ini ++ TAG-00149-Sig-nds ++ TAG-00136-Met-ate  +
E
EU EMA/INS/GCP/856758/ 2018 Guideline on the content, management and archiving of the clinical trial master file (paper and/or electronic) 06-Dec-2018 5.1 - 5.2-001 +
TAG-00126-Cer-rte ++ TAG-00244-Def-ini ++ TAG-00149-Sig-nds ++ TAG-00150-Sou-eUr  +
EU EMA/INS/GCP/856758/ 2018 Guideline on the content, management and archiving of the clinical trial master file (paper and/or electronic) 06-Dec-2018 5.1 - 5.2-002 +
TAG-00126-Cer-rte ++ TAG-00244-Def-ini ++ TAG-00149-Sig-nds ++ TAG-00150-Sou-eUr  +
I
ICH ICH E6 Guideline R3 (2025) III. Annex 1 4.3.3 +
TAG-00127-Com-meC ++ TAG-00129-Dat-ali ++ TAG-00063-Dat-per ++ TAG-00340-Req-nfo  +
ICH ICH E6 Guideline R3 (2025) III. Annex 1 2.12.10 +
TAG-00127-Com-meC ++ TAG-00165-Sys-omb ++ TAG-00246-Inv-hte ++ TAG-00017-Spo-die ++ TAG-00130-Dir-gDi  +
E
EU EMA/INS/GCP/112288/2023 - Guideline on computerised systems and electronic data in clinical trials 2023 4.6 +
TAG-00127-Com-meC ++ TAG-00176-Ris-erh ++ TAG-00246-Inv-hte ++ TAG-00165-Sys-omb  +
W
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - validation +
TAG-00127-Com-meC ++ TAG-00244-Def-ini ++ TAG-00043-Goo-tek  +
I
ICH ICH E6 Guideline R3 (2025) GLOSSARY - Computerised Systems Validation +
TAG-00127-Com-meC ++ TAG-00244-Def-ini ++ TAG-00165-Sys-omb  +
ICH ICH E6 Guideline R3 (2025) III. Annex 1 4.3.8 +
TAG-00127-Com-meC ++ TAG-00294-Rem-gFe ++ TAG-00165-Sys-omb ++ TAG-00123-Bli-ppe  +
G
GBR Guidance Access to Electronic Health Records by Sponsor representatives in clinical trials 44447 System Security +
TAG-00127-Com-meC ++ TAG-00294-Rem-gFe ++ TAG-00063-Dat-per ++ TAG-00017-Spo-die ++ TAG-00137-Mon-che  +
I
ICH ICH E6 Guideline R3 (2025) III. Annex 1 4.3.4 +
TAG-00127-Com-meC ++ TAG-00341-Res-ben ++ TAG-00176-Ris-erh ++ TAG-00165-Sys-omb  +
ICH ICH E6 Guideline R3 (2025) III. Annex 1 4.3 +
TAG-00127-Com-meC ++ TAG-00341-Res-ben ++ TAG-00017-Spo-die ++ TAG-00246-Inv-hte ++ TAG-00343-Doc-ten  +
Retrieved from "https://gxplex.org/index.php?title=Property:RefTags&oldid=20452"