Pages that link to "Glossary:TAG-00341-Res-ben"

The following pages link to Glossary:TAG-00341-Res-ben:

Displaying 29 items.

• Glossary (← links)
• Reference:WHO WHO - HANDBOOK FOR GOOD CLINICAL RESEARCH PRACTICE (GCP) 2005 Overview of the Clinical Research Process (← links)
• Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - 1.5 Regulatory requirements (← links)
• Reference:DEU MBO - Berufsordnung der Ärzt:innen 11-Jun-2021 § 15 (← links)
• Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 11 (← links)
• Reference:DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 77 (← links)
• Reference:DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 85 (← 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 3.2 - Introduction (← links)
• Reference:GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 5-6 (← links)
• Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 6 (← links)
• Reference:USA 21 CFR Part 812 09-Apr-2025 Subpart D (← links)
• Reference:USA 42 CFR Part 11 09-Apr-2025 § 11.4 (← links)
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Sponsor (← links)
• Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 4.17 (← links)
• Reference:N.A. Article from Mora et al. 2023 - (← links)
• Reference:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 6.1 (← links)
• Reference:ICH ICH E6 Guideline R3 (2025) III. Annex 1 4.3 (← links)
• Reference:ICH ICH E6 Guideline R3 (2025) III. Annex 1 4.3.4 (← links)
• Reference:EU EMA/INS/GCP/112288/2023 - Guideline on computerised systems and electronic data in clinical trials 2023 4.2 (← links)
• Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 6 (← links)
• Reference:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 109 Paragraph 1-001 (← links)
• Reference:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 109 Paragraph 1-002 (← links)
• Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 13 (← links)
• Reference:GBR MEDDEV 2.7/3 revision 3 May-2015 5 - 6 (← links)
• Reference:DEU BGB - Bürgerliches Gesetzbuch 22-Dec-2023 § 630 (← links)
• Reference:WMA Declaration of Helsinki 2024 Paragraph 36 (← links)
• Reference:DEU DGEPi - GEP Guter Epidemiologischer Praxis Sep-2018 Leitlinie 10 (← links)