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On 12 June 2009, the European Commission adopted a proposal for a regulation concerning the placing on the market and use of biocidal products. The proposed Regulation will repeal and replace the current Directive 98/8/EC concerning the placing of biocidal products on the market. It will enter into force on January 1, 2013.
EU Biocides Directive Services
Tox Regulatory Affairs can assess your products to determine their current and future compliance status and requirements concerning:
•Data requirements
•What active substances will be phased out
•How will the rules on the inclusion of active substances change
•The main differences between the current directive and the new regulation
Our biocides regulatory compliance solutions include:
•Registration of biocides
•Dossiers preparation for the registration of biocidal substances as prescribed in the Directive both new & old
•Evaluation of existing data and the compilation of a dossier and evaluation of data sets
•Toxicological evaluation support
•Preparation of efficacy data of active substances and non-active substances
•Classification and labelling of biocides according to the CLP regulation
•Preparation and submission of applications for registrations under existing national regulations at Member State level
•Preparation and updating of material safety data sheets (MSDS)
If you would like help with any of the above, or would like further information, please contact us at +45 26 70 96 48 and send questions to info@toxregulatoryaffairs.com
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