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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.
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EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 63 Paragraph 1 +
TAG-00029-Inf-rte ++ TAG-00340-Req-nfo ++ TAG-00028-Leg-ich ++ TAG-00312-Imp-isi ++ TAG-00201-Cli-eSt ++ TAG-00155-Med-Med  +
EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 59 Paragraph 1 +
TAG-00029-Inf-rte ++ TAG-00340-Req-nfo ++ TAG-00028-Leg-ich ++ TAG-00312-Imp-isi ++ TAG-00231-Per-ung  +
EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 29 Paragraph 1 +
TAG-00029-Inf-rte ++ TAG-00340-Req-nfo ++ TAG-00028-Leg-ich ++ TAG-00312-Imp-isi ++ TAG-00149-Sig-nds  +
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USA Informed Consent - FDA Guidance for IRBs, Clinical Investigators, and Sponsors Aug-2023 III. +
TAG-00030-Inf-onu ++ TAG-00029-Inf-rte ++ TAG-00343-Doc-ten ++ TAG-00134-Eth-kom ++ TAG-00320-Foo-eri  +
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EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 29 Paragraph 3-5 +
TAG-00031-Pat-onA ++ TAG-00029-Inf-rte ++ TAG-00028-Leg-ich  +
EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 59 Paragraph 2 +
TAG-00031-Pat-onA ++ TAG-00029-Inf-rte ++ TAG-00028-Leg-ich ++ TAG-00231-Per-ung  +
EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 59 Paragraph 3 – 5 +
TAG-00031-Pat-onA ++ TAG-00029-Inf-rte ++ TAG-00028-Leg-ich ++ TAG-00231-Per-ung  +
EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 63 Paragraph 2 +
TAG-00031-Pat-onA ++ TAG-00029-Inf-rte ++ TAG-00028-Leg-ich ++ TAG-00201-Cli-eSt ++ TAG-00155-Med-Med  +
EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 63 Paragraph 3 – 5 +
TAG-00031-Pat-onA ++ TAG-00029-Inf-rte ++ TAG-00028-Leg-ich ++ TAG-00155-Med-Med  +
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ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 5.8.4 - 5.8.6 +
TAG-00031-Pat-onA ++ TAG-00149-Sig-nds ++ TAG-00029-Inf-rte ++ TAG-00062-Med-tre  +
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WHO WHO - HANDBOOK FOR GOOD CLINICAL RESEARCH PRACTICE (GCP) 2005 Page 60-61 +
TAG-00032-Inf-ngs ++ TAG-00029-Inf-rte ++ TAG-00018-Inv-die ++ TAG-00017-Spo-die ++ TAG-00134-Eth-kom  +
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ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 5.8.2 +
TAG-00032-Inf-ngs ++ TAG-00029-Inf-rte ++ TAG-00019-Pri-Prü ++ TAG-00203-Cli-lin ++ TAG-00201-Cli-eSt  +
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USA Informed Consent - FDA Guidance for IRBs, Clinical Investigators, and Sponsors Aug-2023 II. Introduction +
TAG-00032-Inf-ngs ++ TAG-00029-Inf-rte ++ TAG-00149-Sig-nds ++ TAG-00030-Inf-onu  +
USA Informed Consent - FDA Guidance for IRBs, Clinical Investigators, and Sponsors Aug-2023 II. Advertising-001 +
TAG-00032-Inf-ngs ++ TAG-00083-Enr-enr ++ TAG-00029-Inf-rte ++ TAG-00320-Foo-eri  +
USA Informed Consent - FDA Guidance for IRBs, Clinical Investigators, and Sponsors Aug-2023 II. Advertising-002 +
TAG-00032-Inf-ngs ++ TAG-00083-Enr-enr ++ TAG-00029-Inf-rte ++ TAG-00320-Foo-eri  +
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EU EMA/431265/2016 Annex I – to guidance for the conduct of good clinical practice inspections – investigator site 06-Sep-2017 4. +
TAG-00032-Inf-ngs ++ TAG-00343-Doc-ten ++ TAG-00150-Sou-eUr ++ TAG-00112-Ass-nve ++ TAG-00029-Inf-rte  +
EU EMA/INS/GCP/143492/2022 - ANNEX I TO PROCEDURE FOR CONDUCTING GCP INSPECTIONS REQUESTED BY THE CHMP: INVESTIGATOR SITE 2022 Page 6 +
TAG-00032-Inf-ngs ++ TAG-00343-Doc-ten ++ TAG-00150-Sou-eUr ++ TAG-00112-Ass-nve ++ TAG-00029-Inf-rte  +
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WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Appendix 2 +
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WHO WHO - HANDBOOK FOR GOOD CLINICAL RESEARCH PRACTICE (GCP) 2005 Page 28-29 +
TAG-00033-Pro-oto  +
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EU ENCePP - Guide on Methodological Standards in Pharmacoepidemiology Revision 11 (2023) 3 +
TAG-00033-Pro-oto  +
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