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Domain: All, Subdomain: All documents, EUROVOC descriptor: market approval, Author: European Commission, Search language: English
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Commission Decision (EU) 2020/1184 of 17 July 2020 on the national provisions notified by Hungary pursuant to Article 114(4) of the Treaty on the Functioning of the European Union concerning the cadmium content in phosphate fertilisers (notified under document C(2020) 4862) (Only the Hungarian text is authentic)

C/2020/4862

OJ L 261, 11.8.2020, p. 42–54 (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:
32020D1184
Author:
European Commission, Directorate-General for Internal Market, Industry, Entrepreneurship and SMEs
Date of document:
17/07/2020; Date of adoption

Commission Decision (EU) 2020/1178 of 27 July 2020 on the national provisions notified by the Kingdom of Denmark pursuant to Article 114(4) of the Treaty of the Functioning of the European Union concerning cadmium content in fertilisers (notified under document C(2020) 4988) (Only the Danish text is authentic)

C/2020/4988

OJ L 259, 10.8.2020, p. 14–28 (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:
32020D1178
Author:
European Commission, Directorate-General for Internal Market, Industry, Entrepreneurship and SMEs
Date of document:
27/07/2020; Date of adoption

Commission Implementing Regulation (EU) 2020/1175 of 7 August 2020 concerning the authorisation of L-cysteine hydrochloride monohydrate produced by fermentation with Escherichia coli KCCM 80180 and Escherichia coli KCCM 80181 as a feed additive for all animal species (Text with EEA relevance)

C/2020/5375

OJ L 259, 10.8.2020, p. 6–8 (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:
32020R1175
Author:
European Commission, Directorate-General for Health and Food Safety
Date of document:
07/08/2020; Date of adoption

Commission guidance for the medical devices expert panels on the consistent interpretation of the decision criteria in the clinical evaluation consultation procedure (Text with EEA relevance) 2020/C 259/02

C/2020/5264

OJ C 259, 7.8.2020, p. 2–8 (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:
52020XC0807(01)
Author:
European Commission, Directorate-General for Health and Food Safety
Date of document:
07/08/2020; Date of publication

Commission Implementing Regulation (EU) 2020/1163 of 6 August 2020 authorising the placing on the market of vitamin D2 mushroom powder as a novel food under Regulation (EU) 2015/2283 of the European Parliament and of the Council and amending Commission Implementing Regulation (EU) 2017/2470 (Text with EEA relevance)

C/2020/5305

OJ L 258, 7.8.2020, p. 1–5 (BG, ES, CS, DA, DE, ET, EL, EN, FR, HR, IT, LV, LT, HU, MT, NL, PL, PT, RO, SK, SL, FI, SV)

Date of entry into force unknown (pending notification) or not yet in force.

CELEX number:
32020R1163
Author:
European Commission, Directorate-General for Health and Food Safety
Date of document:
06/08/2020; Date of adoption

Commission Regulation (EU) 2020/1149 of 3 August 2020 amending Annex XVII to Regulation (EC) No 1907/2006 of the European Parliament and of the Council concerning the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH) as regards diisocyanates (Text with EEA relevance)

C/2020/5183

OJ L 252, 4.8.2020, p. 24–27 (BG, ES, CS, DA, DE, ET, EL, EN, FR, HR, IT, LV, LT, HU, MT, NL, PL, PT, RO, SK, SL, FI, SV)

Date of entry into force unknown (pending notification) or not yet in force.

CELEX number:
32020R1149
Author:
European Commission, Directorate-General for Internal Market, Industry, Entrepreneurship and SMEs
Date of document:
03/08/2020; Date of adoption

Commission Implementing Regulation (EU) 2020/1147 of 31 July 2020 granting a Union authorisation for the single biocidal product ‘ClearKlens product based on IPA’ (Text with EEA relevance)

C/2020/5129

OJ L 252, 4.8.2020, p. 1–11 (BG, ES, CS, DA, DE, ET, EL, EN, FR, HR, IT, LV, LT, HU, MT, NL, PL, PT, RO, SK, SL, FI, SV)

Date of entry into force unknown (pending notification) or not yet in force.

CELEX number:
32020R1147
Author:
European Commission, Directorate-General for Health and Food Safety
Date of document:
31/07/2020; Date of adoption

Summary of European Union decisions on marketing authorisations in respect of medicinal products from 1 June 2020 to 30 June 2020 (Decisions taken pursuant to Article 34 of Directive 2001/83/EC or Article 38 of Directive 2001/82/EC)

PUB/2020/588

OJ C 253, 31.7.2020, p. 9–28 (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:
52020XC0731(05)
Author:
European Commission, Directorate-General for Health and Food Safety
Date of document:
31/07/2020; Date of publication

Summary of European Union decisions on marketing authorisations in respect of medicinal products from 1 June 2020 to 30 June 2020 (Published pursuant to Article 13 or Article 38 of Regulation (EC) No 726/2004 of the European Parliament and of the Council)

PUB/2020/587

OJ C 253, 31.7.2020, p. 1–8 (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:
52020XC0731(04)
Author:
European Commission, Directorate-General for Health and Food Safety
Date of document:
31/07/2020; Date of publication
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