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Article, annex, or section this reference covers.
E
EU Regulation (EU) No 520/2012 - performance of pharmacovigilance activities 20-Jun-12 Annex III 2. ; 3. +
Annex III
2. ; 3. +
I
Annex J +
E
Annex VIII +
G
Annex VIII
1. ; 2. +
Annex VIII
1. ; 2. ; 2.2 +
Annex X
2.2 +
Annex X
2.3.7 +
E
EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Annex XIII Part A Section 2.3 +
Annex XIII
Part A
Section 2.3 +
EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Annex XIV Chapter I Section 1.8 +
Annex XIV
Chapter I
Section 1.8 +
EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Annex XIV Chapter II Section 3-001 +
Annex XIV
Chapter II
Section 3 +
EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Annex XIV Chapter II Section 3-002 +
Annex XIV
Chapter II
Section 3 +
EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Annex XIV Chapter II Section 4 +
Annex XIV
Chapter II
Section 4 +
EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Annex XIV Chapter II Section 1.12 +
Annex XIV
Chapter II
Section 1.12 +
EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Annex XIV Chapter II Section 2 +
Annex XIV
Chapter II
Section 2 +
Annex XV
Chapter I
Section 2 +
EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Annex XV Chapter II Section 1.7 +
Annex XV
Chapter II
Section 1.7 +
Annex XV
Chapter III
1. ; 3. +
Annex XV
Chapter III
2. ; 7. +