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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:DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 2 Absatz 3a–4  + (1.2.3)
• Reference:GBR The Medical Devices Regulations 2002 11-Feb-2021 Article 2 in vitro diagnostic medical device  + (1.2.3)
• Reference:GBR The Medical Devices Regulations 2002 11-Feb-2021 Article 2 medical device  + (1.2.3)
• Reference:USA 21 CFR Part 50 09-Apr-2025 § 50.3  + (1.2.3)
• Reference:USA 21 CFR Part 50 09-Apr-2025 § 50.3 (k)-001  + (1.2.3)
• Reference:USA 21 CFR Part 56 09-Apr-2025 § 56.104 (d)  + (1.2.3)
• Reference:USA 45 CFR Part 46 09-Apr-2025 § 46.104  + (1.2.3)
• Reference:USA U.S. Code Title 21 30-Sep-2023 § 321 (f)  + (1.2.3)
• Reference:USA U.S. Code Title 21 30-Sep-2023 § 321 (i)  + (1.2.3)
• Reference:USA U.S. Code Title 21 30-Sep-2023 § 321 (h)  + (1.2.3)
• Reference:USA 21 CFR Part 809 06-May-2024 § 809.3 (a)  + (1.2.3)
• Reference:USA FD&C Act - Federal Food, Drug, and Cosmetic Act 30-Sep-2023 Sec 510 (k)  + (1.2.3)
• Reference:USA FD&C Act - Federal Food, Drug, and Cosmetic Act 30-Sep-2023 Sec 512 (f)  + (1.2.3)
• Reference:USA FD&C Act - Federal Food, Drug, and Cosmetic Act 30-Sep-2023 Sec 737 (8)  + (1.2.3)
• Reference:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 51  + (1.2.4)
• Reference:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Annex VIII  + (1.2.4)
• Reference:EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 47  + (1.2.4)
• Reference:EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Annex VIII  + (1.2.4)
• Reference:DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 6  + (1.2.4)
• Reference:GBR Directive 93/42/EEC 11-Oct-2007 Article 9  + (1.2.4)
• Reference:USA FD&C Act - Federal Food, Drug, and Cosmetic Act 30-Sep-2023 Section 513  + (1.2.4)
• Reference:ICH ICH E8 Guideline R1 (2021) ANNEX: TYPES OF CLINICAL STUDIES  + (1.2.5)
• Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - clinical trial Phases  + (1.2.5)
• Reference:USA 21 CFR Part 312 09-Apr-2025 § 312.21  + (1.2.5)
• Reference:USA 21 CFR Part 312 09-Apr-2025 § 312.85  + (1.2.5)

• Reference:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 Annex I  + (1.2.6)

• Reference:ICH ICH E6 Guideline - Annex 2 R3 Annex 2 Annex 2 3  + (1.2.7)
• Reference:ICH ICH E8 Guideline R1 (2021) -  + (1.2.7)
• Reference:ICH ICH E8 Guideline R1 (2021) 3.3.5  + (1.2.7)
• Reference:ICH ICH E9 Guideline 1998 III  + (1.2.7)
• Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 9.1  + (1.2.7)
• Reference:WHO WHO - HANDBOOK FOR GOOD CLINICAL RESEARCH PRACTICE (GCP) 2005 Overview of the Clinical Research Process  + (1.2.7)
• Reference:EU Recommendations of the expert group - Risk proportionate approaches in clinical trials 25-Apr-2017 2.  + (1.2.7)
• Reference:EU Recommendations of the expert group - Risk proportionate approaches in clinical trials 25-Apr-2017 4.1  + (1.2.7)
• Reference:EU EMA/298712/2022 - Complex clinical trials – Questions and answers 23-May-2022 -  + (1.2.7)
• Reference:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 62 Paragraph 1  + (1.2.7)
• Reference:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 62 Paragraph 3  + (1.2.7)
• Reference:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 74  + (1.2.7)
• Reference:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 82  + (1.2.7)
• Reference:EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 58 Paragraph 1 – 3  + (1.2.7)
• Reference:EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 58 Paragraph 5-001  + (1.2.7)
• Reference:EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 70  + (1.2.7)
• Reference:DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 3 Absatz 4  + (1.2.7)
• Reference:DEU DGEPi - GEP Guter Epidemiologischer Praxis Sep-2018 Leitlinie 2  + (1.2.7)
• Reference:DEU DGEPi - GEP Guter Epidemiologischer Praxis Sep-2018 Leitlinie 3 3.3 - 3.6  + (1.2.7)
• Reference:DEU DGEPi - GEP Guter Epidemiologischer Praxis Sep-2018 Leitlinie 6 6.1  + (1.2.7)
• Reference:USA 21 CFR Part 312 09-Apr-2025 § 312.23 (6) (d)  + (1.2.7)
• Reference:USA 21 CFR Part 314 09-Apr-2025 § 314.126  + (1.2.7)
• Reference:ICH ICH E9 Guideline - Addendum R1 20-Nov-2019 -  + (1.2.8)
• Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 9.3  + (1.2.8)
• Reference:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 Annex A A.7  + (1.2.8)