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Property:RefLanguage

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Showing 20 pages using this property.
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EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 53 +
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EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 77 Paragraph 1, 3 & 4 +
EN  +
EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 80 Paragraph 1-2 +
EN  +
EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 80 Paragraph 3 +
EN  +
EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 80 Paragraph 4 +
EN  +
EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 80 Paragraph 5 – 6 +
EN  +
EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 87 Paragraph 1 – 2 +
EN  +
EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 87 Paragraph 3 – 5 +
EN  +
EU ; GBR MDCG 2020-10/1 - Safety reporting in clinical investigations of medical devices 2020 8-001 +
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EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 76 Paragraph 1 +
EN  +
EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 73 Paragraph 1, 3, 4 +
EN  +
EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 76 Paragraph 2 – 3 +
EN  +
EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 76 Paragraph 4 +
EN  +
EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 76 Paragraph 5 – 6 +
EN  +
EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 82 Paragraph 3 – 5 +
EN  +
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GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 33 +
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GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 34 +
EN  +
GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 35 +
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GBR Directive 2001/20/EC 04-Apr-2001 Article 17 +
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GBR Directive 93/42/EEC 11-Oct-2007 Annex X +
EN  +
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