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Reg. (EU) 2015/1106
Reg. (EU) No 1037/2012
|Old Legislation||Dossier complete 2010/132/EU|
|Date of approval||01/04/2013||Expiration of approval||31/03/2023|
Timelines for submission of confirmatory information amended. Proposal voted at PAFF in June 2015.
The original RMS was UK.
The RMS is Norway
|Type||Candidate for Substitution (CfS)||CfS - criteria||two PBT criteria|
Authorisation at national level
|Authorised in||In progress for|
|AT, BE, BG, CY, CZ, DE, EL, ES, FR, HR, HU, IE, IT, LU, NL, PL, PT, RO, SI, SK, UK||SE|
Classification Reg. 1272/2008
- RMS:Rapporteur Member State
- Co-RMS:Co-Rapporteur Member State
- ADI:Acceptable daily intake
- ARfD:Acute reference dose
- AOEL:Acceptable operator exposure level