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From GxPlex
This page provides a simple browsing interface for finding entities described by a property and a named value. Other available search interfaces include the page property search, and the ask query builder.
List of results
- Reference:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 68 +
- Reference:DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 40b Absatz 1 +
- Reference:DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 40b Absatz 2 +
- Reference:DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 40b Absatz 3 +
- Reference:DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 40b Absatz 4 +
- Reference:DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 40b Absatz 5 +
- Reference:DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 40b Absatz 6-001 +
- Reference:DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 41 +
- Reference:GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Schedule 1 Part 3-002 +
- Reference:GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Schedule 1 Part 4 +
- Reference:GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Schedule 1 Part 5 +
- Reference:USA 21 CFR Part 50 09-Apr-2025 § 50.3 (m) +
- Reference:USA 21 CFR Part 50 09-Apr-2025 § 50.3 (n) +
- Reference:USA 21 CFR Part 50 09-Apr-2025 § 50.3 (o) +
- Reference:USA 21 CFR Part 50 09-Apr-2025 § 50.3 (p) +
- Reference:USA 21 CFR Part 50 09-Apr-2025 § 50.3 (q) +
- Reference:USA 21 CFR Part 50 09-Apr-2025 § 50.3 (r) +
- Reference:USA 21 CFR Part 50 09-Apr-2025 § 50.3 (s) +
- Reference:USA 21 CFR Part 50 09-Apr-2025 Subpart D +
- Reference:USA 45 CFR Part 46 09-Apr-2025 Subpart B +
- Reference:USA 45 CFR Part 46 09-Apr-2025 Subpart C +
- Reference:USA 45 CFR Part 46 09-Apr-2025 Subpart D +
- Reference:USA Informed Consent - FDA Guidance for IRBs, Clinical Investigators, and Sponsors Aug-2023 V. +
- Reference:ICH ICH E6 Guideline R3 (2025) III. Annex 1 2.4.2 +
- Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 4.3 +
- Reference:WHO WHO - HANDBOOK FOR GOOD CLINICAL RESEARCH PRACTICE (GCP) 2005 Page 44 +
- Reference:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 3.42 - recruitment +
- Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 ANNEX I Section K No. 59-60 +
