Documents
675 documents
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Can the Ctgb also reject an authorisation that is received through a mutual recognition procedure?
Yes, rejection is possible based on Articles 36.3, 41.1, and 44 of 1107/2009/EC and Articles 11 and 12 of Directive 2009/128/EC.
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According to the CLP, what are important data for labelling?
Products which have been imported into or produced in the EU and delivered to a third party before June 1, 2015, are considered ...
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Where can I find the guidance documents for CLP on the ECHA site?
You can find the guidance documents for CLP on the ECHA website. See also Understanding CLP.
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Is a label required on a small packaging unit (less than 125 ml)?
No, based on Article 29, the authorisation holder can decide whether to include certain H- and/or P-statements on the label.
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Evaluation Manual v. 2.1/2.2-C
Evaluation Manual version 2.1/2.2-C was published in November 2017 and valid till January 2018. The Evaluation Manual is a ...
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Transitional legislation framework
Product authorisation under transitional legislation The BPR 528/2012 provides a number of transitional measures that allow a ...
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General introduction
The general introduction provides background information on the Biocidal Products Regulation (BPR) for products based on active ...
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European framework
Index: Introduction EU framework Physical-Chemical-Properties Efficacy Human Health Environment In addition to the European ...
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8. Efficacy
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1. General introduction