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Property:RefTags

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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 § 6 +
TAG-00053-Dev-las ++ TAG-00155-Med-Med ++ TAG-00057-Com-deR ++ TAG-00201-Cli-eSt ++ TAG-00231-Per-ung  +
E
EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 51 +
TAG-00053-Dev-las ++ TAG-00155-Med-Med ++ TAG-00176-Ris-erh ++ TAG-00198-Not-Not  +
EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Annex VIII +
TAG-00053-Dev-las ++ TAG-00220-Inv-agn  +
EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 47 +
TAG-00053-Dev-las ++ TAG-00220-Inv-agn ++ TAG-00176-Ris-erh ++ TAG-00198-Not-Not  +
D
DEU DGEPi - GEP Guter Epidemiologischer Praxis Sep-2018 Leitlinie 3 3.3 - 3.6 +
TAG-00054-Stu-ung ++ TAG-00055-Stu-ngs ++ TAG-00010-Non-Stu ++ TAG-00338-Met-odi  +
W
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 9.1 +
TAG-00055-Stu-ngs ++ TAG-00033-Pro-oto ++ TAG-00056-Bio-tik ++ TAG-00145-Ran-ute  +
U
USA 21 CFR Part 312 09-Apr-2025 § 312.23 (6) (d) +
TAG-00055-Stu-ngs ++ TAG-00033-Pro-oto ++ TAG-00011-Inv-tud ++ TAG-00340-Req-nfo  +
W
WHO WHO - Guidance for best practices for clinical trials 2024 2.4 +
TAG-00055-Stu-ngs ++ TAG-00076-Fea-ung ++ TAG-00008-Cli-ngK  +
I
ICH ICH E9 Guideline 1998 III +
TAG-00055-Stu-ngs ++ TAG-00142-Mul-ent ++ TAG-00056-Bio-tik  +
U
USA 42 CFR Part 11 09-Apr-2025 § 11.10 (b) (5) +
TAG-00055-Stu-ngs ++ TAG-00244-Def-ini ++ TAG-00145-Ran-ute ++ TAG-00123-Bli-ppe ++ TAG-00265-Cli-tud  +
USA 21 CFR Part 314 09-Apr-2025 § 314.126 +
TAG-00055-Stu-ngs ++ TAG-00277-Pla-par ++ TAG-00340-Req-nfo ++ TAG-00317-Obj-set  +
E
EU EMA/298712/2022 - Complex clinical trials – Questions and answers 23-May-2022 - +
TAG-00055-Stu-ngs ++ TAG-00302-Ada-die ++ TAG-00338-Met-odi ++ TAG-00056-Bio-tik  +
I
ICH ICH E6 Guideline R3 (2025) Appendix B. B4 +
TAG-00055-Stu-ngs ++ TAG-00304-Pri-tSt ++ TAG-00033-Pro-oto ++ TAG-00123-Bli-ppe ++ TAG-00145-Ran-ute ++ TAG-00277-Pla-par ++ TAG-00302-Ada-die ++ TAG-00011-Inv-tud ++ TAG-00287-Sto-pre ++ TAG-00093-Dru-ent ++ TAG-00099-Ran-ndl ++ TAG-00308-Dec-rüf  +
ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 Annex A A.7 +
TAG-00056-Bio-tik ++ TAG-00055-Stu-ngs  +
ICH ICH E9 Guideline - Addendum R1 20-Nov-2019 - +
TAG-00056-Bio-tik ++ TAG-00305-Sta-Sta ++ TAG-00008-Cli-ngK  +
W
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 9.3 +
TAG-00056-Bio-tik ++ TAG-00305-Sta-Sta ++ TAG-00033-Pro-oto  +
D
DEU DGEPi - GEP Guter Epidemiologischer Praxis Sep-2018 Leitlinie 8 +
TAG-00056-Bio-tik ++ TAG-00338-Met-odi ++ TAG-00073-Arc-arc ++ TAG-00010-Non-Stu  +
DEU DGEPi - GEP Guter Epidemiologischer Praxis Sep-2018 Leitlinie 3 3.9 +
TAG-00056-Bio-tik ++ TAG-00342-Sit-der ++ TAG-00340-Req-nfo ++ TAG-00010-Non-Stu  +
DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 67 (6) +
TAG-00057-Com-deR ++ TAG-00010-Non-Stu ++ TAG-00001-Med-rzn  +
DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 67 (1) ; (6) +
TAG-00057-Com-deR ++ TAG-00010-Non-Stu ++ TAG-00001-Med-rzn ++ TAG-00340-Req-nfo  +
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