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Medicinal products – List of marketing authorisations granted by the EEA EFTA States for the first half of 2020 2021/C 39/04 Subcommittee I on the free movement of goods To be noted by the EEA Joint Committee
Published: 2021-02-04
Subject:
EFTA countries
,
European Economic Area
,
free movement of goods
,
market approval
,
medicament
,
withdrawal from the market
Author
Corporate Author(s):
Standing Committee of the EFTA States
(
European Free Trade Association
)
EU law
PDF
HTML
Permanent link
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)
Published: 2021-01-29
Subject:
drug surveillance
,
EU Member State
,
market approval
,
marketing standard
,
medicament
,
veterinary medicinal product
,
withdrawal from the market
Author
Corporate Author(s):
Directorate-General for Health and Food Safety
(
European Commission
)
;
European Commission
EU law
PDF
HTML
Permanent link
Commission Implementing Decision (EU) 2021/103 of 29 January 2021 not approving carbon dioxide as an existing active substance for use in biocidal products of product-type 19 (Text with EEA relevance)
Published: 2021-01-29
Subject:
carbon
,
insecticide
,
market approval
,
oxide
,
withdrawal from the market
Author
Corporate Author(s):
Directorate-General for Health and Food Safety
(
European Commission
)
;
European Commission
EU law
PDF
HTML
Permanent link
Commission Implementing Decision (EU) 2021/64 of 22 January 2021 authorising the placing on the market of products containing, consisting of or produced from genetically modified soybean SYHT0H2 (SYN-ØØØH2-5), pursuant to Regulation (EC) No 1829/2003 of the European Parliament and of the Council (notified under document C(2021) 266) (Only the Dutch and French texts are authentic) (Text with EEA relevance)
Published: 2021-01-22
Subject:
animal feedingstuffs
,
food safety
,
foodstuff
,
labelling
,
market approval
,
soya bean
,
transgenic plant
Author
Corporate Author(s):
Directorate-General for Health and Food Safety
(
European Commission
)
;
European Commission
EU law
PDF
HTML
Permanent link
Commission Implementing Regulation (EU) 2020/2120 of 16 December 2020 amending Implementing Regulation (EU) 2016/1964 as regards the authorisation of a preparation of montmorillonite-illite as feed additive for all animal species (Text with EEA relevance)
Published: 2020-12-16
Subject:
animal feedingstuffs
,
food additive
,
market approval
Author
Corporate Author(s):
Directorate-General for Health and Food Safety
(
European Commission
)
;
European Commission
EU law
PDF
HTML
Permanent link
Commission Implementing Regulation (EU) 2020/2118 of 16 December 2020 concerning the renewal of the authorisation of Pediococcus pentosaceus DSM 16244 as a feed additive for all animal species and repealing Regulation (EU) No 514/2010 (Text with EEA relevance)
Published: 2020-12-16
Subject:
animal feedingstuffs
,
food additive
,
market approval
Author
Corporate Author(s):
Directorate-General for Health and Food Safety
(
European Commission
)
;
European Commission
EU law
PDF
HTML
Permanent link
EFTA Surveillance Authority Delegated Decision No 151/20/COL of 11 December 2020 establishing a programme of controls for the year 2021 to be carried out in the EEA EFTA States to verify application of EEA legislation in the food and veterinary area [2021/336]
Published: 2020-12-11
Subject:
animal feedingstuffs
,
animal welfare
,
food inspection
,
genetically modified organism
,
Iceland
,
labelling
,
market approval
,
Norway
,
plant health control
,
veterinary inspection
Author
Corporate Author(s):
EFTA Surveillance Authority
(
European Free Trade Association
)
EU law
PDF
HTML
Permanent link
Commission Implementing Regulation (EU) 2020/1643 of 5 November 2020 amending Implementing Regulation (EU) No 540/2011 as regards the approval periods of the active substances calcium phosphide, denathonium benzoate, haloxyfop-P, imidacloprid, pencycuron and zeta-cypermethrin (Text with EEA relevance)
Published: 2020-11-05
Subject:
chemical product
,
market approval
,
plant health control
,
plant health product
Author
Corporate Author(s):
Directorate-General for Health and Food Safety
(
European Commission
)
;
European Commission
EU law
PDF
HTML
Permanent link
Commission Implementing Regulation (EU) 2020/1511 of 16 October 2020 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of the active substances amidosulfuron, bifenox, chlorotoluron, clofentezine, clomazone, cypermethrin, daminozide, deltamethrin, dicamba, difenoconazole, diflufenican, fenoxaprop-P, fenpropidin, fludioxonil, flufenacet, fosthiazate, indoxacarb, lenacil, MCPA, MCPB, nicosulfuron, paraffin oils, picloram, prosulfocarb, sulphur, triflusulfuron and tritosulfuron (Text with EEA relevance)
Published: 2020-10-16
Subject:
market approval
,
plant health control
,
plant health product
Author
Corporate Author(s):
Directorate-General for Health and Food Safety
(
European Commission
)
;
European Commission
EU law
PDF
HTML
Permanent link
Case C-488/20: Request for a preliminary ruling from the Wojewódzki Sąd Administracyjny w Warszawie (Poland) lodged on 2 October 2020 — Delfarma Sp. z o.o. v Prezes Urzędu Rejestracji Produktów Leczniczych, Wyrobów Medycznych i Produktów Biobójczych
Published: 2020-10-02
Subject:
drug surveillance
,
drugs classification
,
import (EU)
,
import licence
,
import restriction
,
market approval
,
medicament
,
quantitative restriction
Author
Corporate Author(s):
Court of Justice
(
Court of Justice of the European Union
)
EU law
PDF
HTML
Permanent link
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