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645 documents
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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
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Data to be submitted for change in production process and/or production location active substance
Data to be submitted for change in production process and/or production location active substance Please note: This appendix must ...
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Evaluation Manual v2.1
Juli 2017 - October 2017 Product authorisation under the BPR The Ctgb regularly publishes Evaluation Manuals, which are technical ...
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Evaluation Manual Biopesticides v1.0
Especially for biopesticides like f.e. botanicals and semiochemicals Ctgb developed an Evaluation Manual. This manual describes ...
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General introduction EM Biocidal products v2.1
The general introduction provides background information on the Biocidal Products Regulation (BPR) for products based on active ...
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Evaluation Manual v2.0/2.1-B
June 2017 Product authorisation under the BPR The Ctgb regularly publishes Evaluation Manuals, which are technical work ...
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Transitional legislation framework Evaluation manual Biocidal Products v2.1
Product authorisation under transitional legislation The BPR 528/2012 provides a number of transitional measures that allow a ...
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European framework Evaluation manual Biocidal Products v2.1
Index: Introduction EU framework Physical-Chemical-Properties Efficacy Human Health Environment In addition to the European ...