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Domain: All, Subdomain: All documents, Legal basis – CELEX number: 32001L0083, Search language: English
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Summary of European Union decisions on marketing authorisations in respect of medicinal products from 1 September 2019 to 30 September 2019 (Decisions taken pursuant to Article 34 of Directive 2001/83/EC or Article 38 of Directive 2001/82/EC)

OJ C 369, 30.10.2019, p. 11–29 (BG, ES, CS, DA, DE, ET, EL, EN, FR, HR, IT, LV, LT, HU, MT, NL, PL, PT, RO, SK, SL, FI, SV)

CELEX number:
52019XC1030(03)
Legal basis:
Author:
European Commission
Date of document:
30/10/2019; Date of publication

Summary of European Union decisions on marketing authorisations in respect of medicinal products from 1 July 2019 to 31 August 2019(Decisions taken pursuant to Article 34 of Directive 2001/83/EC or Article 38 of Directive 2001/82/EC)

OJ C 334, 4.10.2019, p. 17–17 (BG, ES, CS, DA, DE, ET, EL, EN, FR, HR, IT, LV, LT, HU, MT, NL, PL, PT, RO, SK, SL, FI, SV)

CELEX number:
52019XC1004(05)
Legal basis:
Author:
European Commission
Date of document:
04/10/2019; Date of publication

Summary of European Union decisions on marketing authorisations in respect of medicinal products from 1 June 2019 to 30 June 2019 (Decisions taken pursuant to Article 34 of Directive 2001/83/EC or Article 38 of Directive 2001/82/EC)

OJ C 252, 26.7.2019, p. 15–24 (BG, ES, CS, DA, DE, ET, EL, EN, FR, HR, IT, LV, LT, HU, MT, NL, PL, PT, RO, SK, SL, FI, SV)

CELEX number:
52019XC0726(03)
Legal basis:
Author:
European Commission
Date of document:
26/07/2019; Date of publication

Summary of European Union decisions on marketing authorisations in respect of medicinal products from 1 May 2019 to 31 May 2019(Decisions taken pursuant to Article 34 of Directive 2001/83/EC or Article 38 of Directive 2001/82/EC)

OJ C 218, 28.6.2019, p. 8–24 (BG, ES, CS, DA, DE, ET, EL, EN, FR, HR, IT, LV, LT, HU, MT, NL, PL, PT, RO, SK, SL, FI, SV)

CELEX number:
52019XC0628(02)
Legal basis:
Author:
European Commission
Date of document:
28/06/2019; Date of publication

Summary of European Union decisions on marketing authorisations in respect of medicinal products from 1 April 2019 to 30 April 2019 (Decisions taken pursuant to Article 34 of Directive 2001/83/EC or Article 38 of Directive 2001/82/EC)

OJ C 180, 24.5.2019, p. 16–16 (BG, ES, CS, DA, DE, ET, EL, EN, FR, HR, IT, LV, LT, HU, MT, NL, PL, PT, RO, SK, SL, FI, SV)

CELEX number:
52019XC0524(07)
Legal basis:
Author:
European Commission
Date of document:
24/05/2019; Date of publication

Commission Implementing Decision (EU) 2019/769 of 14 May 2019 amending Implementing Decision 2012/715/EU establishing a list of third countries with a regulatory framework applicable to active substances for medicinal products for human use and the respective control and enforcement activities ensuring a level of protection of public health equivalent to that in the Union (Text with EEA relevance.)

C/2019/3482

OJ L 126, 15.5.2019, p. 70–71 (BG, ES, CS, DA, DE, ET, EL, EN, FR, HR, IT, LV, LT, HU, MT, NL, PL, PT, RO, SK, SL, FI, SV)

In force

CELEX number:
32019D0769
Legal basis:
Author:
European Commission, Directorate-General for Health and Food Safety
Date of document:
14/05/2019; Date of adoption

Summary of European Union decisions on marketing authorisations in respect of medicinal products from 1 March 2019 to 31 March 2019 (Decisions taken pursuant to Article 34 of Directive 2001/83/EC 11 or Article 38 of Directive 2001/82/EC 22)

OJ C 153, 3.5.2019, p. 12–229 (BG, ES, CS, DA, DE, ET, EL, EN, FR, HR, IT, LV, LT, HU, MT, NL, PL, PT, RO, SK, SL, FI, SV)

CELEX number:
52019XC0503(06)
Legal basis:
Author:
European Commission
Date of document:
03/05/2019; Date of publication

Summary of European Union decisions on marketing authorisations in respect of medicinal products from 1 January 2019 to 31 January 2019 (Decisions taken pursuant to Article 34 of Directive 2001/83/EC or Article 38 of Directive 2001/82/EC)

OJ C 80, 4.3.2019, p. 11–45 (BG, ES, CS, DA, DE, ET, EL, EN, FR, HR, IT, LV, LT, HU, MT, NL, PL, PT, RO, SK, SL, FI, SV)

CELEX number:
52019XC0304(02)
Legal basis:
Author:
European Commission
Date of document:
04/03/2019; Date of publication

Summary of European Union decisions on marketing authorisations in respect of medicinal products from 1 December 2018 to 31 December 2018 (Decisions taken pursuant to Article 34 of Directive 2001/83/EC or Article 38 of Directive 2001/82/EC)

OJ C 32, 25.1.2019, p. 8–12 (BG, ES, CS, DA, DE, ET, EL, EN, FR, HR, IT, LV, LT, HU, MT, NL, PL, PT, RO, SK, SL, FI, SV)

CELEX number:
52019XC0125(06)
Legal basis:
Author:
European Commission
Date of document:
25/01/2019; Date of publication

Summary of European Union decisions on marketing authorisations in respect of medicinal products from 1 August 2018 to 31 August 2018 (Decisions taken pursuant to Article 34 of Directive 2001/83/EC or Article 38 of Directive 2001/82/EC)

OJ C 349, 28.9.2018, p. 14–19 (BG, ES, CS, DA, DE, ET, EL, EN, FR, HR, IT, LV, LT, HU, MT, NL, PL, PT, RO, SK, SL, FI, SV)

CELEX number:
52018XC0928(04)
Legal basis:
Author:
European Commission
Date of document:
28/09/2018; Date of publication
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