Documents
683 documents
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Cationic polymeric binders with quaternary ammonium compounds to be incorporated in paints – Scope – Art 3(3) BPR Commission Decision
COMMISSION IMPLEMENTING DECISION (EU) 2015/411 of 11 March 2015 pursuant to Article 3(3) of Regulation (EU) No 528/2012 of the ...
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Borderline Biocidal Products Directive 98/8/EC (BPD) and the Plant Protection Products Directive 91/414/EEC (PPPD)
Guidance document agreed between the Commission services and the competent authorities of Member States for the biocidal products ...
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Borderline between the legislation for cosmetics and biocides – endorsed-CA July 2013
This document is an attempt to provide guidance in the interest of consistency, and has been drafted by the Commission services ...
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Bacterial cultures intended to reduce organic solids – Scope – Art 3(3) BPR Commission Decision
COMMISSION IMPLEMENTING DECISION (EU) 2015/646 of 23 April 2015 pursuant to Article 3(3) of Regulation (EU) No 528/2012 of the ...
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Anti-viral tissue impregnated with citric acid – Scope – Art 3(3) BPR Commission Decision
COMMISSION IMPLEMENTING DECISION (EU) 2015/1985 of 4 November 2015 pursuant to Article 3(3) of Regulation (EU) No 528/2012 of the ...
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Disinfection of greenhouses and releated (in Dutch)
From June 2016 on, the Board is on the position that disinfection products used in empty greenhouses or related areas are ...
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Producten op de grensvlakken Warenwet – Wet op de medische hulpmiddelen – Biocidenverordening. M. Woutersen et al, RIVM Rapport 2015-0184 (in Dutch)
Producten op de grensvlakken Warenwet – Wet op de medische hulpmiddelen – Biocidenverordening. M. Woutersen et al, RIVM Rapport ...
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BPR Scope documentation
The Biocidal Products Regulation (EU) 528/2012 (BPR) art.3 defines a ‘biocidal product’as being: “any substance or mixture, in ...
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Note for discussion with Competent Authorities for Biocidal Products may 2015
This document, drafted by the Commission services responsible for biocidal products, is an attempt to provide guidance in the ...
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Introducing new information during the peer review process of active substance approval
Rad ECHA note (january 2016) on Possibility of introducing new data or new information during the peer review process