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Domain: All, Subdomain: All documents, EUROVOC descriptor: medicament, Form: Notice, Search language: English
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Medicinal products — List of marketing authorisations granted by the EEA EFTA States for the first half of 2018

OJ C 68, 21.2.2019, p. 5–26 (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:
E2019G0221(01)
Author:
Standing Committee of the EFTA States
Date of document:
21/02/2019; Date of publication

Medicinal products — List of marketing authorisations granted by the EEA EFTA States for the second half of 2017

OJ C 305, 30.8.2018, p. 15–33 (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:
E2018G0830(02)
Author:
Standing Committee of the EFTA States
Date of document:
30/08/2018; Date of publication

Medicinal products — List of marketing authorisations granted by the EEA EFTA States for the first half of 2017

OJ C 205, 14.6.2018, p. 7–26 (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:
E2018G0614(01)
Author:
Standing Committee of the EFTA States
Date of document:
14/06/2018; Date of publication

Medicinal products — List of marketing authorisations granted by the EEA EFTA States for the second half of 2016

OJ C 195, 7.6.2018, p. 26–43 (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:
E2018G0607(03)
Author:
Standing Committee of the EFTA States
Date of document:
07/06/2018; Date of publication

Summary of European Union decisions on marketing authorisations in respect of medicinal products from 1 October 2017 to 31 October 2017 (Published pursuant to Article 13 or Article 38 of Regulation (EC) No 726/2004 of the European Parliament and of the Council)

OJ C 410, 1.12.2017, p. 1–4 (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:
52017XC1201(03)
Author:
European Commission
Date of document:
01/12/2017; Date of publication

Summary of European Union decisions on marketing authorisations in respect of medicinal products from 1 October 2017 to 31 October 2017 (Decisions taken pursuant to Article 34 of Directive 2001/83/EC or Article 38 of Directive 2001/82/EC)

OJ C 410, 1.12.2017, p. 5–7 (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:
52017XC1201(04)
Author:
European Commission
Date of document:
01/12/2017; Date of publication

Summary of European Union decisions on marketing authorisations in respect of medicinal products from 1 September 2017 to 30 September 2017 (Decisions taken pursuant to Article 34 of Directive 2001/83/EC or Article 38 of Directive 2001/82/EC)

OJ C 367, 27.10.2017, p. 11–108 (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:
52017XC1027(02)
Author:
European Commission
Date of document:
27/10/2017; Date of publication

Summary of European Union decisions on marketing authorisations in respect of medicinal products from 1 September 2017 to 30 September 2017 (Published pursuant to Article 13 or Article 38 of Regulation (EC) No 726/2004 of the European Parliament and of the Council)

OJ C 367, 27.10.2017, p. 1–10 (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:
52017XC1027(01)
Author:
European Commission
Date of document:
27/10/2017; Date of publication

Medicinal products — List of marketing authorisations granted by the EEA EFTA States for the first half of 2016

OJ C 58, 23.2.2017, p. 10–27 (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:
E2017G0223(01)
Author:
Standing Committee of the EFTA States
Date of document:
23/02/2017; Date of publication
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