Pages that link to "Glossary:TAG-00026-Min-isc"
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The following pages link to Glossary:TAG-00026-Min-isc:
Displaying 24 items.
- Glossary (↠links)
- Reference:EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 2 Paragraph 58 (↠links)
- Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 10 (↠links)
- Reference:DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 28 Absatz 4 – 6 (↠links)
- Reference:ICH ICH E6 Guideline R3 (2025) III. Annex 1 1.2.7 (↠links)
- Reference:ICH ICH E6 Guideline R3 (2025) III. Annex 1 2.8.12 (↠links)
- Reference:ICH ICH E11 Guideline R1 (2017) - (↠links)
- Reference:ICH ICH E11 Guideline R1 (2017) 8 (↠links)
- Reference:WHO WHO - HANDBOOK FOR GOOD CLINICAL RESEARCH PRACTICE (GCP) 2005 Page 22 (↠links)
- Reference:WHO WHO - Guidance for best practices for clinical trials 2024 2.1.3 (↠links)
- Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 32 Paragraph 1 (↠links)
- Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 32 Paragraph 2-3 (↠links)
- Reference:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 65 (↠links)
- Reference:DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 40b Absatz 1 (↠links)
- Reference:DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 40b Absatz 3 (↠links)
- Reference:GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Schedule 1 Part 4 (↠links)
- Reference:USA 21 CFR Part 50 09-Apr-2025 § 50.3 (n) (↠links)
- Reference:USA 21 CFR Part 50 09-Apr-2025 § 50.3 (o) (↠links)
- Reference:USA 21 CFR Part 50 09-Apr-2025 § 50.3 (p) (↠links)
- Reference:USA 21 CFR Part 50 09-Apr-2025 § 50.3 (q) (↠links)
- Reference:USA 21 CFR Part 50 09-Apr-2025 § 50.3 (r) (↠links)
- Reference:USA 21 CFR Part 50 09-Apr-2025 Subpart D (↠links)
- Reference:USA 45 CFR Part 46 09-Apr-2025 Subpart D (↠links)
- Reference:USA Informed Consent - FDA Guidance for IRBs, Clinical Investigators, and Sponsors Aug-2023 V. (↠links)
