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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.
D
DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 30-001 +
TAG-00018-Inv-die ++ TAG-00019-Pri-Prü ++ TAG-00244-Def-ini ++ TAG-00017-Spo-die  +
U
USA 21 CFR Part 312 09-Apr-2025 § 312.3 - Investigator +
TAG-00018-Inv-die ++ TAG-00021-Sub-rin ++ TAG-00244-Def-ini ++ TAG-00201-Cli-eSt  +
W
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 1.4 +
TAG-00018-Inv-die ++ TAG-00135-Inv-ntr ++ TAG-00255-Inv-ion ++ TAG-00111-Agr-chr ++ TAG-00151-Sta-rat  +
U
USA 21 CFR Part 312 09-Apr-2025 § 312.70 +
TAG-00018-Inv-die ++ TAG-00143-Non-abw ++ TAG-00320-Foo-eri  +
USA 21 CFR Part 812 09-Apr-2025 § 812.119 +
TAG-00018-Inv-die ++ TAG-00143-Non-abw ++ TAG-00155-Med-Med ++ TAG-00320-Foo-eri  +
I
ICH ICH E6 Guideline R3 (2025) GLOSSARY - Investigator +
TAG-00018-Inv-die ++ TAG-00244-Def-ini ++ TAG-00019-Pri-Prü  +
W
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - investigator +
TAG-00018-Inv-die ++ TAG-00244-Def-ini ++ TAG-00255-Inv-ion  +
U
USA 21 CFR Part 50 09-Apr-2025 § 50.3 (d) +
TAG-00018-Inv-die ++ TAG-00244-Def-ini ++ TAG-00201-Cli-eSt ++ TAG-00001-Med-rzn  +
G
GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 2 investigator +
TAG-00018-Inv-die ++ TAG-00244-Def-ini ++ TAG-00193-Hea-Ang ++ TAG-00135-Inv-ntr  +
U
USA 21 CFR Part 812 09-Apr-2025 § 812.3 (i) +
TAG-00018-Inv-die ++ TAG-00244-Def-ini ++ TAG-00201-Cli-eSt ++ TAG-00155-Med-Med  +
E
EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 49 +
TAG-00018-Inv-die ++ TAG-00255-Inv-ion ++ TAG-00135-Inv-ntr ++ TAG-00340-Req-nfo  +
I
ICH ICH E6 Guideline R3 (2025) III. Annex 1 2 +
TAG-00018-Inv-die ++ TAG-00255-Inv-ion ++ TAG-00334-Tra-ngP ++ TAG-00340-Req-nfo  +
W
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 4.2 +
TAG-00018-Inv-die ++ TAG-00255-Inv-ion ++ TAG-00043-Goo-tek ++ TAG-00062-Med-tre  +
E
EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 58 Paragraph 7 – 8 +
TAG-00018-Inv-die ++ TAG-00255-Inv-ion ++ TAG-00231-Per-ung ++ TAG-00100-Lab-bor  +
U
USA 21 CFR Part 54 09-Apr-2025 § 54.4 disclosure +
TAG-00018-Inv-die ++ TAG-00320-Foo-eri ++ TAG-00017-Spo-die ++ TAG-00343-Doc-ten  +
D
DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 30-002 +
TAG-00019-Pri-Prü ++ TAG-00018-Inv-die ++ TAG-00244-Def-ini ++ TAG-00017-Spo-die  +
W
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - principal investigator +
TAG-00019-Pri-Prü ++ TAG-00244-Def-ini ++ TAG-00142-Mul-ent  +
D
DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 3 Absatz 5 – 6 +
TAG-00019-Pri-Prü ++ TAG-00244-Def-ini ++ TAG-00018-Inv-die ++ TAG-00142-Mul-ent  +
G
GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 2 (1) +
TAG-00019-Pri-Prü ++ TAG-00244-Def-ini ++ TAG-00135-Inv-ntr ++ TAG-00142-Mul-ent  +
I
ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 10.2 +
TAG-00019-Pri-Prü ++ TAG-00255-Inv-ion ++ TAG-00334-Tra-ngP ++ TAG-00201-Cli-eSt  +
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