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1 September 2016: Transitional period deadline for treated articles

1 September 2016: Transitional period deadline for treated articles

Have you already confirmed whether the biocidal active substance you use is already approved or under evaluation for the relevant product-type? Are your products labelled correctly? According to the Biocidal Products Regulation (BPR), articles can be treated with, or intentionally incorporating during manufacturing, one or more biocidal products as long as the active substance/s are […]

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New version of R4BP 3 coming in July

New version of R4BP 3 coming in July

New version of R4BP 3 (the dossier submission tool supporting the Biocidal Products Regulation) coming in July The launch date for the new version of R4BP 3 is planned for the 5th of July 2016.  As recommended by ECHA (ECHA/NA/16/19), those companies which are preparing biocide dossiers in IUCLID 5 should submit their dossiers through […]

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New version of IUCLID available (IUCLID 6)

New version of IUCLID available (IUCLID 6)

A new version of IUCLID used for creating biocides and REACH dossiers has been published on the 29th of April. As recommended by ECHA (ECHA/NA/16/19), those companies which are preparing REACH dossiers in IUCLID 5 should submit their dossiers before 21 June 2016. However, the biocide dossier in IUCLID 5 can be submitted until the […]

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Kaeltia Biocide Consortium

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Kaeltia Biocide Consortium

We are pleased to announce that KAELTIA has developed an IT System, called KBC (KAELTIA Biocide Consortium) that facilitates manufacturers/formulators/distributors of biocidal products to work together and to cooperate in the preparation of EU authorisation dossiers under the Regulation 528/2012. We invite you to visit KBC website http://consortium.kaeltia.com/ and to check teh User Guide of this System. […]

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