Pages that link to "Glossary:TAG-00038-Ear-tig"

The following pages link to Glossary:TAG-00038-Ear-tig:

Displaying 26 items.

• Glossary (← links)
• Reference:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 77 Paragraph 1, 3 & 4 (← links)
• Reference:EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 73 Paragraph 1, 3, 4 (← links)
• Reference:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 77 (← links)
• Reference:GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 31 (← links)
• Reference:GBR Directive 93/42/EEC 11-Oct-2007 Article 15 6. - 7.-001 (← links)
• Reference:USA 21 CFR Part 312 09-Apr-2025 § 312.44 (d) (← links)
• Reference:USA 21 CFR Part 312 09-Apr-2025 § 312.56 (← links)
• Reference:ICH ICH E6 Guideline R3 (2025) III. Annex 1 2.6 (← links)
• Reference:ICH ICH E6 Guideline R3 (2025) III. Annex 1 3.17.1 (← links)
• Reference:ICH ICH E9 Guideline 1998 4.5 (← links)
• Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 4.15 (← links)
• Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 5.14 (← links)
• Reference:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 8.2 (← links)
• Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 2 Paragraph 26 - 29 (← links)
• Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 37 Paragraph 1 – 7 (← links)
• Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 38 (← links)
• Reference:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 77 Paragraph 1 – 3 (← links)
• Reference:GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Schedule 5 (5) (← links)
• Reference:USA 45 CFR Part 46 09-Apr-2025 § 46.123 (← links)
• Reference:USA 21 CFR Part 312 09-Apr-2025 § 312.38 (← links)
• Reference:USA 21 CFR Part 312 09-Apr-2025 § 312.44 (← links)
• Reference:USA 21 CFR Part 812 09-Apr-2025 § 812.3 (q) (← links)
• Reference:USA 21 CFR Part 812 09-Apr-2025 § 812.46 (b) - (c)-002 (← links)
• Reference:ICH ICH E6 Guideline R3 (2025) III. Annex 3.17.2 (← links)
• Reference:EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 73 Paragraph 5 (← links)