Pages that link to "Template:ReferenceData"
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The following pages link to Template:ReferenceData:
Displaying 50 items.
- Reference:ICH ICH E6 Guideline R3 (2025) III. Annex 1 1.2.7 (transclusion) (← links)
- Reference:ICH ICH E6 Guideline R3 (2025) III. Annex 1 2.8.12 (transclusion) (← links)
- Reference:ICH ICH E6 Guideline R3 (2025) III. Annex 1 2.8.13 (transclusion) (← links)
- Reference:ICH ICH E6 Guideline R3 (2025) III. Annex 1 2.8.8 (transclusion) (← links)
- Reference:ICH ICH E6 Guideline R3 (2025) II 2.4 (transclusion) (← links)
- Reference:ICH ICH E21 Concept paper 2023 2. (transclusion) (← links)
- Reference:CIOMS CIOMS - International Ethical Guidelines for Health-related Research Involving Humans 2016 GUIDELINE 19 (transclusion) (← links)
- Reference:CIOMS CIOMS - International Ethical Guidelines for Health-related Research Involving Humans 2016 GUIDELINE 18 (transclusion) (← links)
- Reference:ICH ICH E11 Guideline R1 (2017) - (transclusion) (← links)
- Reference:ICH ICH E11 Guideline R1 (2017) 8 (transclusion) (← links)
- Reference:ICH ICH E7 Guideline 1993 - (transclusion) (← links)
- Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 3.3 e) - g) (transclusion) (← links)
- Reference:WHO WHO - HANDBOOK FOR GOOD CLINICAL RESEARCH PRACTICE (GCP) 2005 Page 22 (transclusion) (← links)
- Reference:WHO WHO - Guidance for best practices for clinical trials 2024 2.1.3 (transclusion) (← links)
- Reference:WMA Declaration of Helsinki 2024 Paragraph 29 – 30 (transclusion) (← links)
- Reference:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 3.55 (transclusion) (← links)
- Reference:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 5.7 (transclusion) (← links)
- Reference:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 5.8.3 (transclusion) (← links)
- Reference:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 5.8.4 - 5.8.6 (transclusion) (← links)
- Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 31 Paragraph 1 (transclusion) (← links)
- Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 31 Paragraph 2-3 (transclusion) (← links)
- Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 32 Paragraph 1 (transclusion) (← links)
- Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 32 Paragraph 2-3 (transclusion) (← links)
- Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 33 (transclusion) (← links)
- Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 35 Paragraph 1 (transclusion) (← links)
- Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 35 Paragraph 2-3 (transclusion) (← links)
- Reference:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 64 (transclusion) (← links)
- Reference:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 65 (transclusion) (← links)
- Reference:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 66 (transclusion) (← links)
- Reference:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 68 (transclusion) (← links)
- Reference:DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 40b Absatz 1 (transclusion) (← links)
- Reference:DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 40b Absatz 2 (transclusion) (← links)
- Reference:DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 40b Absatz 3 (transclusion) (← links)
- Reference:DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 40b Absatz 4 (transclusion) (← links)
- Reference:DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 40b Absatz 5 (transclusion) (← links)
- Reference:DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 40b Absatz 6-001 (transclusion) (← links)
- Reference:DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 41 (transclusion) (← links)
- Reference:GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Schedule 1 Part 3-002 (transclusion) (← links)
- Reference:GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Schedule 1 Part 4 (transclusion) (← links)
- Reference:GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Schedule 1 Part 5 (transclusion) (← links)
- Reference:USA 21 CFR Part 50 09-Apr-2025 § 50.3 (m) (transclusion) (← links)
- Reference:USA 21 CFR Part 50 09-Apr-2025 § 50.3 (n) (transclusion) (← links)
- Reference:USA 21 CFR Part 50 09-Apr-2025 § 50.3 (o) (transclusion) (← links)
- Reference:USA 21 CFR Part 50 09-Apr-2025 § 50.3 (p) (transclusion) (← links)
- Reference:USA 21 CFR Part 50 09-Apr-2025 § 50.3 (q) (transclusion) (← links)
- Reference:USA 21 CFR Part 50 09-Apr-2025 § 50.3 (r) (transclusion) (← links)
- Reference:USA 21 CFR Part 50 09-Apr-2025 § 50.3 (s) (transclusion) (← links)
- Reference:USA 21 CFR Part 50 09-Apr-2025 Subpart D (transclusion) (← links)
- Reference:USA 45 CFR Part 46 09-Apr-2025 Subpart B (transclusion) (← links)
- Reference:USA 45 CFR Part 46 09-Apr-2025 Subpart C (transclusion) (← links)