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Informal consolidated version of:REGULATION (EC) No 1221/2009 OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL of 25 November 2009 on the voluntary participation by organizations in a Community comanagement

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What is eur-lex - 32009r1221?

Eur-lex - 32009r1221 refers to a specific regulation of the European Union that establishes guidelines for the approval and marketing of biocidal products within EU member states.

Who is required to file eur-lex - 32009r1221?

Manufacturers and importers of biocidal products are required to file information in accordance with eur-lex - 32009r1221.

How to fill out eur-lex - 32009r1221?

To fill out eur-lex - 32009r1221, applicants must follow the specific guidelines provided in the regulation, which includes providing detailed information regarding the product, its active substances, and safety data.

What is the purpose of eur-lex - 32009r1221?

The purpose of eur-lex - 32009r1221 is to regulate the placing on the market of biocidal products, ensuring they meet safety and efficacy standards to protect human health and the environment.

What information must be reported on eur-lex - 32009r1221?

The information that must be reported includes product details, chemical composition, efficacy data, safety assessments, and information regarding labeling and instructions for safe use.