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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:EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 2 Paragraph 4 – 6  + (Article 2 Paragraph 4 – 6)
• Reference:EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 2 Paragraph 42  + (Article 2 Paragraph 42)
• Reference:EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 2 Paragraph 45  + (Article 2 Paragraph 45)
• Reference:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 2 Paragraph 57 – 59  + (Article 2 Paragraph 57 – 59)
• Reference:EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 2 Paragraph 58  + (Article 2 Paragraph 58)
• Reference:EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 2 Paragraph 60 – 62  + (Article 2 Paragraph 60 – 62)
• Reference:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 2 Paragraph 64 – 66  + (Article 2 Paragraph 64 – 66)
• Reference:EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 2 Paragraph 67–69  + (Article 2 Paragraph 67–69)
• Reference:EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 2 Paragraph 7 – 9  + (Article 2 Paragraph 7 – 9)
• Reference:GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 2 (1)  + (Article 2 (1))
• Reference:GBR Directive 2001/20/EC 04-Apr-2001 Article 2 (a)  + (Article 2 (a))
• Reference:GBR Directive 2001/20/EC 04-Apr-2001 Article 2 (c)  + (Article 2 (c))
• Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 20 Paragraph 1-3  + (Article 20 Paragraph 1-3)
• Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 20 Paragraph 4-7  + (Article 20 Paragraph 4-7)
• Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 21  + (Article 21)
• Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 22  + (Article 22)
• Reference:GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 22-23  + (Article 22-23)
• Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 23 Paragraph 1-2  + (Article 23 Paragraph 1-2)
• Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 23 Paragraph 3-6  + (Article 23 Paragraph 3-6)
• Reference:FRA Constitution du 4 octobre 1958 10-Mar-2024 Article 24  + (Article 24)
• Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 24  + (Article 24)
• Reference:GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 24  + (Article 24)
• Reference:GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 25  + (Article 25)
• Reference:EU Regulation (EC) No 726/2004 - authorisation and supervision of medicinal products for human use 28-Jan-22 Article 26  + (Article 26)
• Reference:GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 27  + (Article 27)

• Reference:GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 28  + (Article 28)

• Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 28 Paragraph 1  + (Article 28 Paragraph 1)
• Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 28 Paragraph 1 (f)  + (Article 28 Paragraph 1 (f))
• Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 28 Paragraph 2-3  + (Article 28 Paragraph 2-3)
• Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 29 Paragraph 1  + (Article 29 Paragraph 1)
• Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 29 Paragraph 2  + (Article 29 Paragraph 2)
• Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 29 Paragraph 3-5  + (Article 29 Paragraph 3-5)
• Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 29 Paragraph 6-8  + (Article 29 Paragraph 6-8)
• Reference:GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 29A  + (Article 29A)
• Reference:GBR Directive 2001/20/EC 04-Apr-2001 Article 3  + (Article 3)
• Reference:GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 3 (1) - (5)  + (Article 3 (1) - (5))
• Reference:GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 3 (6) - (11)  + (Article 3 (6) - (11))
• Reference:EU Regulation (EU) 910/2014 - electronic identification 17-Sep-2014 Article 3 Paragraph 10  + (Article 3 Paragraph 10)
• Reference:GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 30-001  + (Article 30)
• Reference:GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 30-002  + (Article 30)
• Reference:GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 31  + (Article 31)
• Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 31 Paragraph 1  + (Article 31 Paragraph 1)
• Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 31 Paragraph 2-3  + (Article 31 Paragraph 2-3)
• Reference:GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 32  + (Article 32)
• Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 32 Paragraph 1  + (Article 32 Paragraph 1)
• Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 32 Paragraph 2-3  + (Article 32 Paragraph 2-3)
• Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 33  + (Article 33)
• Reference:GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 33  + (Article 33)
• Reference:FRA Constitution du 4 octobre 1958 10-Mar-2024 Article 34  + (Article 34)
• Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 34  + (Article 34)
• Reference:GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 34  + (Article 34)