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Property:RefUnit

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Unit number this reference belongs to.

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Showing 20 pages using this property.
E
EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 82 Paragraph 3 – 5 +
5.3.5  +
D
DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 40b Absatz 6-002 +
5.3.6  +
DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 40d-003 +
5.3.6  +
DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 63 +
5.3.6  +
DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 64 +
5.3.6  +
A
AUT MPG – Medizinproduktegesetz 26-May-2022 § 22 +
5.3.6  +
F
FRA AEC DOC012 v03 Avis aux promoteurs d’investigations cliniques de DM (RIPH1) – Partie II 16-May-2025 3. +
5.3.6  +
FRA AEC DOC012 v03 Avis aux promoteurs d’investigations cliniques de DM (RIPH1) – Partie II 16-May-2025 2.-001 +
5.3.6  +
FRA SURV VIG DOC118 V01 REC-Avis aux promoteurs -Partie V 16-May-2025 5. +
5.3.6  +
FRA Code de la Santé Publique - Partie Réglementaire - 1ere partie, Livre 1er, Titre II 16-May-2025 R1123-46 +
5.3.6  +
FRA Code de la Santé Publique - Partie Réglementaire - 1ere partie, Livre 1er, Titre II 16-May-2025 R1123-53 +
5.3.6  +
G
GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 33 +
5.3.6  +
GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 34 +
5.3.6  +
GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 35 +
5.3.6  +
GBR Directive 2001/20/EC 04-Apr-2001 Article 17 +
5.3.6  +
GBR Directive 93/42/EEC 11-Oct-2007 Annex X +
5.3.6  +
GBR Clinical investigations of medical devices – compiling a submission to MHRA May 2021 2.-002 +
5.3.6  +
E
EU ; GBR MDCG 2020-10/1 - Safety reporting in clinical investigations of medical devices 2020 8-002 +
5.3.6  +
G
GBR MEDDEV 2.7/3 revision 3 May-2015 4 +
5.3.6  +
GBR MEDDEV 2.7/3 revision 3 May-2015 5 - 6 +
5.3.6  +
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