Top Most 15+ Art 71 Of Directive 2001/83/ec

1.[PDF] B DIRECTIVE 2001/83/EC OF THE EUROPEAN PARLIAMENT AND ...

DIRECTIVE 2001/83/EC OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL of 6 November 2001 ... medicinal product by applying the criteria listed in Article 71.

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2.[PDF] Directive 2001/83/ec Of The European Parliament And Of The

6 nov. 2001 · (5) Article 71 of Council Regulation (EEC) No. 2309/93 of 22 July 1993 laying down Community procedures for the authorisation and supervision of ...

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3.Directive 2001/83/EC Of The European ... - .uk

Article 71U.K. · 1.Medicinal products shall be subject to medical prescription where they: · 2.Where Member States provide for the sub-category of medicinal ...

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4.Directive 2001/83/EC Of The European ... - .uk

Article 71.(1) Medicinal products shall be subject to medical prescription where... Article 72.Medicinal products not ...

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5.Directive 2001/83/EC Of The European Parliament And ... - EU Monitor

The provisions of this Directive shall apply to industrially produced medicinal products for human use intended to be placed on the market in Member States.

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6.Directive 2004/27/ec Of The European Parliament And Of The Council

amending Directive 2001/83/EC on the Community code relating to medicinal products for human ... (5) Article 71 of Council Regulation (EEC) No 2309/93 of.

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7.Directive 2001/83/EC

Directive 2001/83/EC of the European Parliament and of the Council of 6 November 2001 On the Community code relating to medicinal products for human use.

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8.[DOC] 2. Marketing Authorisation/registration Application Particulars

A mutual recognition procedure (according to Article 28(2) of Directive 2001/83/EC). Reference Member State: Date of authorisation/registration: ...

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9.[PDF] JUDGMENT OF THE COURT 15 July 2021* (Directive 2001/83/EC

15 juil. 2021 · 71 While it is for the referring court to ascertain, in the light of the facts of the main proceedings, whether the conditions of Article 3(2) ...

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10.Legislation On The Preparation Of Medicinal Products In European ...

The ECJ first clarified the scope of Directive 2001/83/EC as determined in article 2. The Directive applies to medicinal products for human use intended to be ...

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11.Tag Archives: MDR – Article 71 – Assessment By Member States

components of animal or human origin or of substances, which maybe considered medicinal products in accordance with Directive 2001/83/EC.

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12.Article 117: Amendment To Directive 2001/83/EC

In Annex I to Directive 2001/83/EC, point 12 of Section 3.2. is replaced by the following: '(12) Where, in accordance with the second subparagraph of Article 1( ...

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13.Does The Directive 2001/83/Ec Protect Such A Right For The End User?

5 juil. 2022 · In the Directive 2001/83/EC relating to pharmaceuticals for human use all the ... This article will scrutinise the level of legal protection.

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14.[PDF] Community Code Relating To Medicinal Products For Human Use

Article 1, point 5 (Directive 2001/83/EC). (ba) Point (5) is replaced by the following: "(5) Homeopathic medicinal product: Any medicinal product prepared ...

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15.[PDF] B DIRECTIVE 2001/83/EC OF THE EUROPEAN PARLIAMENT AND ...

6 nov. 2001 · DIRECTIVE 2001/83/EC OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL ... medicinal product by applying the criteria listed in Article 71.

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Top Most 15+ Art 71 Of Directive 2001/83/ec

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