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EFSA has launched a public consultation on its draft guidance for the preparation and presentation of applications for authorisation of infant or follow-on formulae manufactured from protein hydrolysates.
The guidance document specifies what kind of information and data applicants need to submit. It covers applications for the assessment of the safety and suitability of the specific formula and applications on the formula’s efficacy in reducing the risk of infants becoming allergic to milk proteins.
EFSA invites interested parties to submit written comments by 3 March 2017.
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