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European Union
Commission Implementing Regulation (EU) 2022/944
Chapter I
Article 5
1.
(a)

Commission Implementing Regulation (EU) 2022/944

law://eu/reg/2022/944/art_5__para_1__pnt_a@2026-11-15

Version in force onWhereEuropean Union

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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

Contents

1. EU reference laboratories shall have a confidentiality pol…
2. EU reference laboratories shall put in place and document…

Contents

1. EU reference laboratories shall have a confidentiality pol…
2. EU reference laboratories shall put in place and document…

This text since 10 Jul 2022

In force

(a)the type of information that shall be considered confidential;

Source: EUR-Lex, © European Union, 1998-2026. Reuse authorised under Decision 2011/833/EU.

Connections

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