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European Union
Commission Implementing Regulation (EU) 2022/944
Chapter I
Article 4
3.
(a)

Commission Implementing Regulation (EU) 2022/944

In forceThis text since 10 Jul 2022law://eu/reg/2022/944/art_4__para_3__pnt_a@2026-11-12

Version in force onWhereEuropean Union

1. The EU reference laboratories shall identify at least one…
2. The EU reference laboratories shall have sufficient admini…
3. The EU reference laboratories shall establish and keep up-…

Contents

1. The EU reference laboratories shall identify at least one…
2. The EU reference laboratories shall have sufficient admini…
3. The EU reference laboratories shall establish and keep up-…

(a)evidence of their status as a legal entity;

Key facts

Type: Implementing regulation · Commission Implementing Regulation (EU) 2022/944 · EEA relevant
Adopted: 17 Jun 2022
In force: 10 Jul 2022
Made by: Directorate-General for Health and Food Safety, European Commission
Official: EUR-Lex 32022R0944 · ELI

Topics

application of EU law EU reference laboratory international standard medical device operation of the Institutions professional qualifications research body rules of procedure sampling testing Internal market - Principles Medical devices

History · 1 version

10 Jul 2022Reading

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Cited by 2: Commission Implementing Regulation (EU) 2022/945; this act