| | Scope | Document part | Language | Document |
|---|
| EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 77 Paragraph 4 – 5 | MD | Article 77
Paragraph 4 – 5 | EN | EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 |
| EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 73 Paragraph 5 | IVD | Article 73
Paragraph 5 | EN | EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 |
| EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 77 Paragraph 4 – 5 | IVD | Article 77
Paragraph 4 – 5 | EN | EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 |
| EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 2 Paragraph 26 - 29 | HM | Article 2
Paragraph 26 - 29 | EN | EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 |
| EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 37 Paragraph 1 – 7 | HM | Article 37
Paragraph 1 – 7 | EN | EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 |
| EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 37 Paragraph 4 | HM | Article 37
Paragraph 4 | EN | EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 |
| GBR Directive 2001/20/EC 04-Apr-2001 Article 10 (c) | HM | Article 10
(c) | EN | GBR Directive 2001/20/EC 04-Apr-2001 |
| GBR The Medical Devices Regulations 2002 11-Feb-2021 Article 16 (11) | MD | Article 16
(11) | EN | GBR The Medical Devices Regulations 2002 11-Feb-2021 |
| GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 27 | HM | Article 27 | EN | GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 |
| GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Schedule 3 Part 1 1. (p) | HM | Schedule 3
Part 1
1. (p) | EN | GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 |
