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.
I
ICH ICH E6 Guideline R3 (2025) GLOSSARY - Randomisation +
TAG-00145-Ran-ute ++ TAG-00244-Def-ini  +
ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 3.42 - randomization +
TAG-00145-Ran-ute ++ TAG-00244-Def-ini ++ TAG-00155-Med-Med ++ TAG-00202-Inv-Pro  +
ICH ICH E6 Guideline R3 (2025) GLOSSARY - Service Provider +
TAG-00147-Ser-inD ++ TAG-00244-Def-ini ++ TAG-00017-Spo-die ++ TAG-00018-Inv-die  +
U
USA FDA Guidance for Industry - Oversight of Clinical Investigations — A Risk-Based Approach to Monitoring Aug-2013 VI C. +
TAG-00148-Con-rsc ++ TAG-00137-Mon-che ++ TAG-00245-Spo-ten ++ TAG-00320-Foo-eri ++ TAG-00144-Qua-gew  +
I
ICH ICH E6 Guideline R3 (2025) GLOSSARY - Contract Research Organisation (CRO) +
TAG-00148-Con-rsc ++ TAG-00244-Def-ini ++ TAG-00147-Ser-inD  +
U
USA 21 CFR Part 312 09-Apr-2025 § 312.3 (b) - CRO +
TAG-00148-Con-rsc ++ TAG-00244-Def-ini ++ TAG-00017-Spo-die ++ TAG-00320-Foo-eri ++ TAG-00137-Mon-che  +
W
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - contract research organization (CRO) +
TAG-00148-Con-rsc ++ TAG-00244-Def-ini ++ TAG-00017-Spo-die ++ TAG-00111-Agr-chr  +
U
USA 21 CFR Part 312 09-Apr-2025 § 312.52 +
TAG-00148-Con-rsc ++ TAG-00245-Spo-ten ++ TAG-00017-Spo-die ++ TAG-00111-Agr-chr  +
I
ICH ICH E6 Guideline R3 (2025) GLOSSARY - Signature +
TAG-00149-Sig-nds ++ TAG-00244-Def-ini  +
U
USA FDA Guidance for Industry - Computerized Systems Used in Clinical Trials 13-Apr-2015 III +
TAG-00150-Sou-eUr ++ TAG-00064-Ele-eUn ++ TAG-00073-Arc-arc ++ TAG-00343-Doc-ten  +
USA FDA Guidance for Industry - Computerized Systems Used in Clinical Investigations May-2007 IV +
TAG-00150-Sou-eUr ++ TAG-00064-Ele-eUn ++ TAG-00272-Ret-enA ++ TAG-00135-Inv-ntr ++ TAG-00320-Foo-eri  +
E
EU EMA/INS/GCP/126568/2023 - Annual Report of the Good Clinical Practice (GCP) Inspectors' Working Group (IWG) 2022 2023 3.1.2 - SD +
TAG-00150-Sou-eUr ++ TAG-00118-Cri-rit ++ TAG-00119-Maj-heF ++ TAG-00327-Exa-spi ++ TAG-00343-Doc-ten  +
U
USA FDA Guidance for Industry - Electronic Source Data in Clinical Investigations Sep-2013 II +
TAG-00150-Sou-eUr ++ TAG-00129-Dat-ali ++ TAG-00320-Foo-eri ++ TAG-00340-Req-nfo  +
I
ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 7.5.3 +
TAG-00150-Sou-eUr ++ TAG-00201-Cli-eSt ++ TAG-00257-Sit-zen  +
W
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - raw data +
TAG-00150-Sou-eUr ++ TAG-00244-Def-ini ++ TAG-00100-Lab-bor  +
E
EU EMA/INS/GCP/112288/2023 - Guideline on computerised systems and electronic data in clinical trials 2023 4.4 +
TAG-00150-Sou-eUr ++ TAG-00244-Def-ini ++ TAG-00129-Dat-ali  +
I
ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 3.47 +
TAG-00150-Sou-eUr ++ TAG-00244-Def-ini ++ TAG-00201-Cli-eSt  +
W
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - patient/subject file +
TAG-00150-Sou-eUr ++ TAG-00244-Def-ini ++ TAG-00124-Cas-Prü ++ TAG-00025-Sub-mer  +
I
ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 3.48 +
TAG-00150-Sou-eUr ++ TAG-00244-Def-ini ++ TAG-00126-Cer-rte ++ TAG-00201-Cli-eSt  +
ICH ICH E6 Guideline R3 (2025) GLOSSARY - Source Records +
TAG-00150-Sou-eUr ++ TAG-00244-Def-ini ++ TAG-00126-Cer-rte ++ TAG-00136-Met-ate ++ TAG-00310-Pat-ien  +
Retrieved from "https://gxplex.org/index.php?title=Property:RefTags&oldid=20452"