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Property:RefTags

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

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Showing 20 pages using this property.
U
USA FDA - HUMAN DRUG CGMP NOTES Volume 8, Number 3 6 +
TAG-00132-Goo-rst ++ TAG-00343-Doc-ten ++ TAG-00320-Foo-eri ++ TAG-00035-Man-odu  +
W
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 7.1 - Committee +
TAG-00133-Ind-rhe ++ TAG-00045-Adv-hte ++ TAG-00329-Saf-lne ++ TAG-00137-Mon-che  +
I
ICH ICH E6 Guideline R3 (2025) GLOSSARY - Independent Data Monitoring Committee (IDMC) +
TAG-00133-Ind-rhe ++ TAG-00244-Def-ini ++ TAG-00329-Saf-lne ++ TAG-00017-Spo-die  +
ICH ICH E9 Guideline 1998 Glossary - IDMC +
TAG-00133-Ind-rhe ++ TAG-00244-Def-ini ++ TAG-00329-Saf-lne ++ TAG-00017-Spo-die  +
W
WHO WHO - HANDBOOK FOR GOOD CLINICAL RESEARCH PRACTICE (GCP) 2005 Page 78 +
TAG-00133-Ind-rhe ++ TAG-00244-Def-ini ++ TAG-00329-Saf-lne ++ TAG-00303-Int-lan  +
I
ICH ICH E6 Guideline R3 (2025) III. Annex 1 3.9 +
TAG-00133-Ind-rhe ++ TAG-00315-Spo-des ++ TAG-00329-Saf-lne ++ TAG-00017-Spo-die  +
D
DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 41 +
TAG-00134-Eth-kom ++ TAG-00008-Cli-ngK ++ TAG-00057-Com-deR ++ TAG-00001-Med-rzn  +
G
GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 15 (5) (d) +
TAG-00134-Eth-kom ++ TAG-00018-Inv-die ++ TAG-00257-Sit-zen  +
GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 14 +
TAG-00134-Eth-kom ++ TAG-00019-Pri-Prü ++ TAG-00059-Reg-lat  +
GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 16 +
TAG-00134-Eth-kom ++ TAG-00019-Pri-Prü ++ TAG-00059-Reg-lat  +
D
DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 35 +
TAG-00134-Eth-kom ++ TAG-00021-Sub-rin ++ TAG-00142-Mul-ent ++ TAG-00019-Pri-Prü  +
G
GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 15 (7) - (10) +
TAG-00134-Eth-kom ++ TAG-00027-Inc-son ++ TAG-00154-Vul-eil ++ TAG-00029-Inf-rte  +
I
ICH ICH E6 Guideline R3 (2025) III. Annex 1 2.4.2 +
TAG-00134-Eth-kom ++ TAG-00033-Pro-oto ++ TAG-00029-Inf-rte ++ TAG-00246-Inv-hte ++ TAG-00083-Enr-enr  +
D
DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 40 +
TAG-00134-Eth-kom ++ TAG-00040-Sub-Änd ++ TAG-00322-Fed-imi ++ TAG-00017-Spo-die  +
DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 41 +
TAG-00134-Eth-kom ++ TAG-00040-Sub-Änd ++ TAG-00018-Inv-die ++ TAG-00135-Inv-ntr  +
W
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 3.2 - Responsibility +
TAG-00134-Eth-kom ++ TAG-00041-Ame-run ++ TAG-00046-Ser-sSc ++ TAG-00051-Eth-ngs ++ TAG-00033-Pro-oto  +
C
CIOMS CIOMS - International Ethical Guidelines for Biomedical Research Involving Human Subjects 2016 Page 20 +
TAG-00134-Eth-kom ++ TAG-00051-Eth-ngs ++ TAG-00033-Pro-oto  +
W
WMA Declaration of Helsinki 2024 Paragraph 23 +
TAG-00134-Eth-kom ++ TAG-00051-Eth-ngs ++ TAG-00033-Pro-oto ++ TAG-00340-Req-nfo  +
D
DEU DGEPi - GEP Guter Epidemiologischer Praxis Sep-2018 Leitlinie 1 1.1 ; 1.3 +
TAG-00134-Eth-kom ++ TAG-00051-Eth-ngs ++ TAG-00010-Non-Stu ++ TAG-00340-Req-nfo  +
U
USA Expedited Review: Categories of Research that may be Reviewed Through an Expedited Review Procedure 1998 - +
TAG-00134-Eth-kom ++ TAG-00052-Ris-ein ++ TAG-00327-Exa-spi ++ TAG-00001-Med-rzn ++ TAG-00155-Med-Med  +
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