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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

article  61

CELEX:  02012R0528-20240611

Letter of access
1. A letter of access shall contain at least the following information:
(a) the name and contact details of the data owner and the beneficiary;
(b) the name of the active substance or biocidal product for which access to the data is authorised;
(c) the date on which the letter of access takes effect;
(d) a list of the submitted data to which the letter of access grants citation rights.
2. 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.