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European Union
Commission Implementing Regulation (EU) 2025/2086
Article 3
2.
(b)

Commission Implementing Regulation (EU) 2025/2086

law://eu/reg/2025/2086/art_3__para_2__pnt_b@2026-11-13

Version in force onWhereEuropean Union

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Key facts

Type: Implementing regulation · Commission Implementing Regulation (EU) 2025/2086
Adopted: 17 Oct 2025
In force: 9 Nov 2025
Made by: Directorate-General for Health and Food Safety, European Commission
Official: EUR-Lex 32025R2086 · ELI

Topics

clinical trial exchange of information health technology medical device scientific cooperation Public health Research and technological development

Contents

1. The HTA secretariat shall invite the health technology dev…
2. The HTA secretariat shall invite the health technology dev…
3. If the subgroup of the Coordination Group on joint clinica…
4. The information listed in paragraph 1 may be provided by r…

Contents

1. The HTA secretariat shall invite the health technology dev…
2. The HTA secretariat shall invite the health technology dev…
3. If the subgroup of the Coordination Group on joint clinica…
4. The information listed in paragraph 1 may be provided by r…

History · 1 version

9 Nov 2025Reading

This text since 9 Nov 2025

In force

(b)receipt of the request from the HTA secretariat referred to in Article 2(1), point (b).

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

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Cites 1: this act