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AFACERI ŞI CONCURENŢĂ
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Summary of European Union decisions on marketing authorisations in respect of medicinal products from 1 December 2020 to 31 December 2020 (Published pursuant to Article 13 or Article 38 of Regulation (EC) No 726/2004 of the European Parliament and of the Council)
Publicat(ă) la: 2021-01-29
Subiecte:
drug surveillance
,
EU Member State
,
market approval
,
marketing standard
,
medicament
,
veterinary medicinal product
,
withdrawal from the market
Author
Autor(i) colectiv(i):
Directorate-General for Health and Food Safety
(
Comisia Europeană
)
;
European Commission
Dreptul UE
PDF
HTML
Link permanent
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)
Publicat(ă) la: 2020-07-31
Subiecte:
drug surveillance
,
EU Member State
,
market approval
,
marketing standard
,
medicament
,
withdrawal from the market
Author
Autor(i) colectiv(i):
Directorate-General for Health and Food Safety
(
Comisia Europeană
)
;
European Commission
Dreptul UE
PDF
HTML
Link permanent
Communication from the Commission Guidelines on the adoption of Union-wide derogations for medical devices in accordance with Article 59 of Regulation (EU) 2017/745 2020/C 171/01
Publicat(ă) la: 2020-05-19
Subiecte:
derogation from EU law
,
EC conformity marking
,
epidemic
,
health legislation
,
infectious disease
,
market approval
,
marketing standard
,
medical device
,
quality standard
,
safety standard
Author
Autor(i) colectiv(i):
Directorate-General for Health and Food Safety
(
Comisia Europeană
)
;
European Commission
Dreptul UE
PDF
HTML
Link permanent
Summary of European Commission Decisions on authorisations for the placing on the market for the use and/or for use of substances listed in Annex XIV to Regulation (EC) No 1907/2006 of the European Parliament and of the Council concerning the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH) (Published pursuant to Article 64(9) of Regulation (EC) No 1907/2006 (OJ L 396, 30.12.2006, p. 1.)) (Text with EEA relevance) 2020/C 130/04
Publicat(ă) la: 2020-04-21
Subiecte:
chemical process
,
chemical product
,
chromium
,
health control
,
health risk
,
market approval
,
marketing standard
,
metal coating
Author
Autor(i) colectiv(i):
Directorate-General for Internal Market, Industry, Entrepreneurship and SMEs
(
Comisia Europeană
)
;
European Commission
Dreptul UE
PDF
HTML
Link permanent
Summary of European Commission Decisions on authorisations for the placing on the market for the use and/or for use of substances listed in Annex XIV to Regulation (EC) No 1907/2006 of the European Parliament and of the Council concerning the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH) (Published pursuant to Article 64(9) of Regulation (EC) No 1907/2006 (OJ L 396, 30.12.2006, p. 1.)) (Text with EEA relevance) 2020/C 122/03
Publicat(ă) la: 2020-04-15
Subiecte:
chemical compound
,
chemical product
,
health control
,
health risk
,
market approval
,
marketing standard
,
metal coating
Author
Autor(i) colectiv(i):
Directorate-General for Internal Market, Industry, Entrepreneurship and SMEs
(
Comisia Europeană
)
;
European Commission
Dreptul UE
PDF
HTML
Link permanent
Case T-113/20: Action brought on 20 February 2020 — BSEF v Commission
Publicat(ă) la: 2020-02-20
Subiecte:
electronic device
,
energy efficiency
,
environmental impact
,
equal treatment
,
halogen
,
marketing standard
,
principle of legal certainty
,
principle of proportionality
,
rights of the defence
,
screen
Author
Autor(i) colectiv(i):
General Court
(
Curtea de Justiție a Uniunii Europene
)
Dreptul UE
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Summary of European Union decisions on marketing authorisations in respect of medicinal products from 1 March 2019 to 31 March 2019 (Published pursuant to Article 13 or Article 38 of Regulation (EC) No 726/2004 of the European Parliament and of the Council 1 1 )
Publicat(ă) la: 2019-05-03
Subiecte:
drug surveillance
,
EU Member State
,
market approval
,
marketing standard
,
medicament
,
veterinary medicinal product
Author
Autor(i) colectiv(i):
European Commission
Dreptul UE
PDF
HTML
Link permanent
Information on the assessment of technical files of established geographical indications for spirit drinks
Publicat(ă) la: 2019-03-27
Subiecte:
consumer information
,
designation of origin
,
EU Member State
,
labelling
,
marketing standard
,
product designation
,
spirits
,
technical specification
Author
Autor(i) colectiv(i):
European Commission
Dreptul UE
PDF
HTML
Link permanent
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)
Publicat(ă) la: 2019-03-04
Subiecte:
drug surveillance
,
EU Member State
,
market approval
,
marketing standard
,
medicament
Author
Autor(i) colectiv(i):
European Commission
Dreptul UE
PDF
HTML
Link permanent
Summary of European Commission Decisions on authorisations for the placing on the market for the use and/or for use of substances listed in Annex XIV to Regulation (EC) No 1907/2006 of the European Parliament and of the Council concerning the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH) (Published pursuant to Article 64(9) of Regulation (EC) No 1907/2006) (Text with EEA relevance.)
Publicat(ă) la: 2019-02-21
Subiecte:
chemical product
,
chromium
,
health control
,
health risk
,
market approval
,
marketing standard
,
metal coating
,
oxide
Author
Autor(i) colectiv(i):
Directorate-General for Internal Market, Industry, Entrepreneurship and SMEs
(
Comisia Europeană
)
;
European Commission
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