Choose the experimental features you want to try

This document is an excerpt from the EUR-Lex website

Document C2006/108/04

    Case C-84/06: Reference for a preliminary ruling from the Hoge Raad der Nederlanden, lodged on 10 February 2006 — Staat der Nederlanden (Ministerie van Volksgezondheid, Welzijn en Sport) v 1. Antroposana, Patiëntenvereniging voor Antroposofische Gezondheidszorg, 2. Nederlandse Vereniging van Antroposofische Artsen, 3. Weleda Nederland NV and 4. Wala Nederland NV

    OB C 108, 6.5.2006, p. 3–3 (ES, CS, DA, DE, ET, EL, EN, FR, IT, LV, LT, HU, NL, PL, PT, SK, SL, FI, SV)

    6.5.2006   

    EN

    Official Journal of the European Union

    C 108/3


    Reference for a preliminary ruling from the Hoge Raad der Nederlanden, lodged on 10 February 2006 — Staat der Nederlanden (Ministerie van Volksgezondheid, Welzijn en Sport) v 1. Antroposana, Patiëntenvereniging voor Antroposofische Gezondheidszorg, 2. Nederlandse Vereniging van Antroposofische Artsen, 3. Weleda Nederland NV and 4. Wala Nederland NV

    (Case C-84/06)

    (2006/C 108/04)

    Language of the case: Dutch

    Referring court

    Hoge Raad der Nederlanden (Supreme Court of the Netherlands)

    Parties to the main proceedings

    Applicant: Staat der Nederlanden (Ministerie van Volksgezondheid, Welzijn en Sport) (State of the Netherlands (Ministry of Public Health, Welfare and Sport))

    Defendants: 1. Antroposana, Patiëntenvereniging voor Antroposofische Gezondheidszorg, 2. Nederlandse Vereniging van Antroposofische Artsen, 3. Weleda Nederland NV and 4. Wala Nederland NV

    Questions referred

    1.

    Does Directive 2001/83/EC (1) of the European Parliament and of the Council of 6 November 2001 on the Community code relating to medicinal products for human use oblige Member States to make anthroposophic medicinal products which are not at the same time homeopathic medicinal products subject to the requirements in respect of authorisation as set out in Title III, Chapter 1, of that directive?

    2.

    If the answer to Question 1 is in the negative: is the Netherlands statutory provision which makes those anthroposophic medicinal products subject to the aforementioned requirements in respect of authorisation an exception to the prohibition under Article 28 EC which is authorised by virtue of Article 30 EC?


    (1)  OJ L 311, p. 67.


    Top