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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.
W
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 6.2 +
TAG-00020-Cli-nit ++ TAG-00135-Inv-ntr ++ TAG-00342-Sit-der ++ TAG-00100-Lab-bor ++ TAG-00080-Sit-uch  +
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 6 +
TAG-00020-Cli-nit ++ TAG-00137-Mon-che ++ TAG-00341-Res-ben ++ TAG-00334-Tra-ngP ++ TAG-00135-Inv-ntr  +
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - monitor +
TAG-00020-Cli-nit ++ TAG-00244-Def-ini ++ TAG-00137-Mon-che ++ TAG-00017-Spo-die ++ TAG-00148-Con-rsc  +
U
USA 21 CFR Part 812 09-Apr-2025 § 812.3 (j) +
TAG-00020-Cli-nit ++ TAG-00244-Def-ini ++ TAG-00017-Spo-die ++ TAG-00148-Con-rsc ++ TAG-00155-Med-Med  +
USA 21 CFR Part 312 09-Apr-2025 § 312.53 (d) +
TAG-00020-Cli-nit ++ TAG-00245-Spo-ten ++ TAG-00334-Tra-ngP ++ TAG-00017-Spo-die ++ TAG-00320-Foo-eri  +
E
EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Annex XIV Chapter II Section 4 +
TAG-00020-Cli-nit ++ TAG-00245-Spo-ten ++ TAG-00232-Per-die ++ TAG-00043-Goo-tek ++ TAG-00231-Per-ung  +
EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Annex XV Chapter III Section 4 +
TAG-00020-Cli-nit ++ TAG-00245-Spo-ten ++ TAG-00203-Cli-lin ++ TAG-00043-Goo-tek ++ TAG-00155-Med-Med  +
U
USA 21 CFR Part 312 09-Apr-2025 § 312.53 (viii) +
TAG-00021-Sub-rin ++ TAG-00011-Inv-tud ++ TAG-00340-Req-nfo ++ TAG-00320-Foo-eri  +
A
AUT BASG - FAQ 11-Feb-2025 Änderung am Personal +
TAG-00021-Sub-rin ++ TAG-00042-Non-ügi ++ TAG-00257-Sit-zen ++ TAG-00326-Fed-wes ++ TAG-00340-Req-nfo  +
I
ICH ICH E6 Guideline R3 (2025) GLOSSARY - Sub-Investigator +
TAG-00021-Sub-rin ++ TAG-00244-Def-ini ++ TAG-00248-Inv-die  +
N
N.A. Article from Mora et al. 2023 - +
TAG-00022-Stu-erS ++ TAG-00341-Res-ben ++ TAG-00075-Pub-ich  +
I
ICH ICH E6 Guideline R3 (2025) III. Annex 1 2.9.1 +
TAG-00025-Sub-mer ++ TAG-00029-Inf-rte ++ TAG-00086-Fol-Fol ++ TAG-00033-Pro-oto  +
ICH ICH E8 Guideline R1 (2021) 6.2.2 +
TAG-00025-Sub-mer ++ TAG-00033-Pro-oto ++ TAG-00287-Sto-pre ++ TAG-00329-Saf-lne  +
U
USA 21 CFR Part 50 09-Apr-2025 § 50.3 (g) +
TAG-00025-Sub-mer ++ TAG-00244-Def-ini ++ TAG-00001-Med-rzn  +
USA 45 CFR Part 46 09-Apr-2025 § 46.102 (e) (1) +
TAG-00025-Sub-mer ++ TAG-00244-Def-ini ++ TAG-00104-Bio-sch  +
USA 21 CFR Part 812 09-Apr-2025 § 812.3 (p) +
TAG-00025-Sub-mer ++ TAG-00244-Def-ini ++ TAG-00202-Inv-Pro ++ TAG-00155-Med-Med  +
D
DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 40b Absatz 1 +
TAG-00026-Min-isc ++ TAG-00027-Inc-son ++ TAG-00029-Inf-rte ++ TAG-00028-Leg-ich ++ TAG-00008-Cli-ngK  +
G
GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Schedule 1 Part 4 +
TAG-00026-Min-isc ++ TAG-00028-Leg-ich ++ TAG-00029-Inf-rte ++ TAG-00112-Ass-nve  +
E
EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 65 +
TAG-00026-Min-isc ++ TAG-00029-Inf-rte ++ TAG-00028-Leg-ich ++ TAG-00112-Ass-nve ++ TAG-00201-Cli-eSt  +
EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 32 Paragraph 1 +
TAG-00026-Min-isc ++ TAG-00029-Inf-rte ++ TAG-00028-Leg-ich ++ TAG-00112-Ass-nve ++ TAG-00008-Cli-ngK  +
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