Article 61

Regulation (EU) No 528/2012 of the European Parliament and of the Council of 22 May 2012 concerning the making available on the market and use of biocidal products Text with EEA relevance · European Union

A letter of access shall contain at least the following information: the name and contact details of the data owner and the beneficiary; the name of the active substance or biocidal product for which access to the data is authorised; the date on which the letter of access takes effect; a list of the submitted data to which the letter of access grants citation rights. Revocation of a letter of access shall not affect the validity of the authorisation issued on the basis of the letter of access in question.

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Source: EUR-Lex (Cellar) · retrieved 2026-10-29 · Text as adopted (Official Journal); later amendments are not incorporated in this text.