Pages that link to "Glossary:TAG-00134-Eth-kom"
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The following pages link to Glossary:TAG-00134-Eth-kom:
Displaying 50 items.
- Glossary (↠links)
- Reference:WHO WHO - HANDBOOK FOR GOOD CLINICAL RESEARCH PRACTICE (GCP) 2005 WHO Principles of GCP (↠links)
- Reference:USA 21 CFR Part 56 09-Apr-2025 § 56.110 (a) - (b) (1) (↠links)
- Reference:USA Expedited Review: Categories of Research that may be Reviewed Through an Expedited Review Procedure 1998 - (↠links)
- Reference:USA 21 CFR Part 56 09-Apr-2025 § 56.104 (d) (↠links)
- Reference:USA 45 CFR Part 46 09-Apr-2025 § 46.104 (↠links)
- Reference:WHO WHO - HANDBOOK FOR GOOD CLINICAL RESEARCH PRACTICE (GCP) 2005 Overview of the Clinical Research Process (↠links)
- Reference:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 62 Paragraph 3 (↠links)
- Reference:EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 58 Paragraph 5-001 (↠links)
- Reference:DEU MBO - Berufsordnung der Ärzt:innen 11-Jun-2021 § 15 (↠links)
- Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Institutional Review Board (IRB)/Independent Ethics Committee (IEC) (↠links)
- Reference:ICH ICH E6 Guideline R3 (2025) III. Annex 1 1 (↠links)
- Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - ethics committee (↠links)
- Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 3.2 - Introduction (↠links)
- Reference:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 3.24 (↠links)
- Reference:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 3.26 (↠links)
- Reference:WMA Declaration of Helsinki 2024 Paragraph 23 (↠links)
- Reference:CIOMS CIOMS - International Ethical Guidelines for Biomedical Research Involving Human Subjects 2016 Page 20 (↠links)
- Reference:DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 41a (↠links)
- Reference:DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 41b (↠links)
- Reference:DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 41c (↠links)
- Reference:DEU KPBV - Klinische Prüfung-Bewertungsverfahren-Verordnung 31-Jan-2022 § 4 (↠links)
- Reference:DEU KPBV - Klinische Prüfung-Bewertungsverfahren-Verordnung 31-Jan-2022 § 5 (↠links)
- Reference:DEU DGEPi - GEP Guter Epidemiologischer Praxis Sep-2018 Leitlinie 1 1.1 ; 1.3 (↠links)
- Reference:GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 2 relevant ethics committee (↠links)
- Reference:GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 5-6 (↠links)
- Reference:GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 7-10 (↠links)
- Reference:USA 21 CFR Part 50 09-Apr-2025 § 50.3 (i) (↠links)
- Reference:USA 21 CFR Part 312 09-Apr-2025 § 312.3 - IEC (↠links)
- Reference:USA 21 CFR Part 812 09-Apr-2025 § 812.3 (f) (↠links)
- Reference:USA 21 CFR Part 812 09-Apr-2025 § 812.3 (t) (↠links)
- Reference:USA 21 CFR Part 56 09-Apr-2025 - (↠links)
- Reference:USA 21 CFR Part 56 09-Apr-2025 Subpart B (↠links)
- Reference:USA 21 CFR Part 56 09-Apr-2025 Subpart C (↠links)
- Reference:USA 45 CFR Part 46 09-Apr-2025 § 46.107 - § 46.112 (↠links)
- Reference:USA 45 CFR Part 46 09-Apr-2025 § 46.115 (↠links)
- Reference:USA 45 CFR Part 46 09-Apr-2025 Subpart E (↠links)
- Reference:ICH ICH E6 Guideline R3 (2025) III. Annex 1 3.8 (↠links)
- Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 3.2 - Consultation (↠links)
- Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 4 (↠links)
- Reference:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 62 Paragraph 3 & 4 (↠links)
- Reference:DEU KPBV - Klinische Prüfung-Bewertungsverfahren-Verordnung 31-Jan-2022 § 6 (↠links)
- Reference:DEU KPBV - Klinische Prüfung-Bewertungsverfahren-Verordnung 31-Jan-2022 § 7 (↠links)
- Reference:DEU KPBV - Klinische Prüfung-Bewertungsverfahren-Verordnung 31-Jan-2022 § 10 (↠links)
- Reference:DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 35 (↠links)
- Reference:DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 31 (↠links)
- Reference:DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 33 (↠links)
- Reference:DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 48 (↠links)
- Reference:DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 49 (↠links)
- Reference:DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 50 (↠links)
