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.
D
DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 68 +
TAG-00044-Ins-ion ++ TAG-00057-Com-deR ++ TAG-00201-Cli-eSt ++ TAG-00231-Per-ung  +
DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 79 +
TAG-00044-Ins-ion ++ TAG-00057-Com-deR ++ TAG-00329-Saf-lne ++ TAG-00343-Doc-ten  +
W
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 11.2 +
TAG-00044-Ins-ion ++ TAG-00057-Com-deR ++ TAG-00135-Inv-ntr ++ TAG-00150-Sou-eUr  +
E
EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 78 +
TAG-00044-Ins-ion ++ TAG-00057-Com-deR ++ TAG-00340-Req-nfo ++ TAG-00334-Tra-ngP  +
D
DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 77 +
TAG-00044-Ins-ion ++ TAG-00057-Com-deR ++ TAG-00201-Cli-eSt ++ TAG-00155-Med-Med  +
W
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 4.12-003 +
TAG-00044-Ins-ion ++ TAG-00113-Aud-tQu ++ TAG-00137-Mon-che ++ TAG-00246-Inv-hte  +
A
AUT BASG - FAQ 11-Feb-2025 Schwarz +
TAG-00044-Ins-ion ++ TAG-00152-Tri-gat ++ TAG-00343-Doc-ten ++ TAG-00326-Fed-wes ++ TAG-00124-Cas-Prü  +
E
EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 72 Pragraph 5 +
TAG-00044-Ins-ion ++ TAG-00201-Cli-eSt ++ TAG-00135-Inv-ntr ++ TAG-00203-Cli-lin  +
EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 68 Paragraph 5 +
TAG-00044-Ins-ion ++ TAG-00231-Per-ung ++ TAG-00135-Inv-ntr  +
G
GBR Directive 2001/20/EC 04-Apr-2001 Article 2 (l) +
TAG-00044-Ins-ion ++ TAG-00244-Def-ini ++ TAG-00057-Com-deR ++ TAG-00144-Qua-gew  +
I
ICH ICH E6 Guideline R3 (2025) GLOSSARY - Inspection +
TAG-00044-Ins-ion ++ TAG-00244-Def-ini ++ TAG-00057-Com-deR ++ TAG-00135-Inv-ntr ++ TAG-00017-Spo-die  +
W
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - inspection +
TAG-00044-Ins-ion ++ TAG-00244-Def-ini ++ TAG-00043-Goo-tek ++ TAG-00113-Aud-tQu  +
U
USA 21 CFR Part 312 09-Apr-2025 § 312.68 +
TAG-00044-Ins-ion ++ TAG-00320-Foo-eri ++ TAG-00018-Inv-die ++ TAG-00343-Doc-ten  +
USA 21 CFR Part 812 09-Apr-2025 § 812.145 +
TAG-00044-Ins-ion ++ TAG-00320-Foo-eri ++ TAG-00017-Spo-die ++ TAG-00155-Med-Med ++ TAG-00018-Inv-die  +
USA 21 CFR Part 312 09-Apr-2025 § 312.58 +
TAG-00044-Ins-ion ++ TAG-00320-Foo-eri ++ TAG-00017-Spo-die ++ TAG-00343-Doc-ten  +
G
GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 2 adverse event adverse reaction +
TAG-00045-Adv-hte ++ TAG-00003-Adv-cht ++ TAG-00244-Def-ini ++ TAG-00001-Med-rzn  +
U
USA 21 CFR Part 312 09-Apr-2025 § 312.32 - Life-threatening Adverse event +
TAG-00045-Adv-hte ++ TAG-00003-Adv-cht ++ TAG-00244-Def-ini ++ TAG-00069-Imm-rhe ++ TAG-00258-Ser-nfü  +
USA NCI GUIDELINES FOR INVESTIGATORS: ADVERSE EVENT REPORTING REQUIREMENTS FOR DCTD (CTEP AND CIP) INDs AND IDEs 30-Aug-2024 5.2 +
TAG-00045-Adv-hte ++ TAG-00029-Inf-rte ++ TAG-00252-Exp-hle ++ TAG-00033-Pro-oto  +
E
EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 ANNEX I Section D No. 19 +
TAG-00045-Adv-hte ++ TAG-00046-Ser-sSc ++ TAG-00033-Pro-oto ++ TAG-00250-Inv-sme ++ TAG-00258-Ser-nfü  +
W
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 5.13 +
TAG-00045-Adv-hte ++ TAG-00046-Ser-sSc ++ TAG-00245-Spo-ten ++ TAG-00017-Spo-die ++ TAG-00250-Inv-sme  +
Retrieved from "https://gxplex.org/index.php?title=Property:RefTags&oldid=20452"