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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:ICH ICH E6 Guideline R3 (2025) III. Annex 1 3.8  +
• Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 3.2 - Consultation  +
• Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 4.8 - 4.9  +
• Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 4  +
• Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 5  +
• Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 6  +
• Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 7  +
• Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 8  +
• Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 9  +
• Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 10  +
• Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 11  +
• Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 12  +
• Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 13  +
• Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 14  +
• Reference:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 62 Paragraph 3 & 4  +
• Reference:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 70 Paragraph 1  +
• Reference:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 70 Paragraph 6 – 7  +
• Reference:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 73  +
• Reference:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Annex XV Chapter II Section 1.7  +
• Reference:EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 57  +
• Reference:EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 58  +
• Reference:EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 66 Paragraph 1  +
• Reference:EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 66 Paragraph 6 – 7  +
• Reference:EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 69  +
• Reference:EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Annex XIV Chapter I Section 1.8  +
• Reference:EU Directive 2001/83/EC - Community code relating to medicinal products for human use 20-Jun-12 Article 107m (1)  +
• Reference:EU Directive 2001/83/EC - Community code relating to medicinal products for human use 20-Jun-12 Article 107n  +
• Reference:EU Regulation (EC) No 726/2004 - authorisation and supervision of medicinal products for human use 28-Jan-22 Article 26  +
• Reference:DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 40  +
• Reference:DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 40a  +
• Reference:DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 40b-001  +
• Reference:DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 40c-001  +
• Reference:DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 42a  +
• Reference:DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 63 g Absatz 3  +
• Reference:DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 67 (1) ; (6)  +
• Reference:DEU KPBV - Klinische Prüfung-Bewertungsverfahren-Verordnung 31-Jan-2022 § 6  +
• Reference:DEU KPBV - Klinische Prüfung-Bewertungsverfahren-Verordnung 31-Jan-2022 § 7  +
• Reference:DEU KPBV - Klinische Prüfung-Bewertungsverfahren-Verordnung 31-Jan-2022 § 10  +
• Reference:DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 35  +
• Reference:DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 31  +
• Reference:DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 31a  +
• Reference:DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 31b  +
• Reference:DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 33  +
• Reference:DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 38  +
• Reference:DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 39  +
• Reference:DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 47-002  +
• Reference:DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 48  +
• Reference:DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 49  +
• Reference:DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 50  +
• Reference:DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 53  +