Commission Regulation (EU) No 1141/2010

In force

This text since 1 Jan 2021law://eu/reg/2010/1141/art_15__para_1@2026-11-14

Contents

1.After receiving the renewal assessment report, the Authority shall immediately communicate it for comments to the applicant and to the Member States. Such comments shall be communicated to the Authority within 2 months, which shall collate and forward those comments, including its own, to the Commission.

Source: EUR-Lex, © European Union, 1998-2026. Reuse authorised under Decision 2011/833/EU.

Key facts

Type: Regulation · Commission Regulation (EU) No 1141/2010 · EEA relevant
Adopted: 7 Dec 2010
In force: 28 Dec 2010
Text current to: 1 Jan 2021
Made by: European Commission
Official: EUR-Lex 32010R1141 · ELI

Topics

chemical product environmental protection EU Member State evaluation method exchange of information pharmaceutical product plant health product Plant health legislation

History · 1 version

1 Jan 2021Reading

Connections

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Cited by 9: Commission Regulation (EU) No 284/2013; Sipcam Oxon SpA v European Commission (T-518/19); FMC Corporation v European Commission (T-719/17)9 provisions; this act2 provisions; Antony C. Tweedale v European Food Safety Authority (T-716/14)3 provisions; Heidi Hautala and Others v European Food Safety Authority (T-329/17); Commission Regulation (EU) 2015/14753 provisions; Commission Implementing Regulation (EU) No 380/20132 provisions; Commission Implementing Regulation (EU) 2019/3363 provisions

Defined terms · 6

Show every defined term

applicant
means a producer who applies for the renewal of the inclusion of an active substance referred to in column A of Annex I;
co-rapporteur Member State
means a Member State which cooperates in the evaluation carried out by the rapporteur Member State, as listed in column C of Annex I for the respective active substance;
inclusion
means inclusion of an active substance in Annex I to Directive 91/414/EEC;
producer
means the person who manufactures the active substance on his own or who contracts out the manufacturing to another party or a person designated by the manufacturer as his sole representative for the purpose of compliance with this Regulation;
rapporteur Member State
means the Member State which evaluates an active substance, as listed in column B of Annex I for the respective active substance;
renewal
means renewal of the inclusion of an active substance in Annex I to Directive 91/414/EEC.