Our team at ECT responsible for services around biocidal products is experienced in preparing and reviewing dossier documents according to the Biocidal Products Directive (BPD, 98/8/EC) such as documents I-IV as well as the IUCLID datasets of various product types (PT). We have specialised in the areas of ecotoxicology, chemical fate and behaviour, and physico-chemical properties. Other dossier sections can also be handled at ECT or are covered by our partners.

Our expertise includes exposure and risk assessments by using appropriate Emission Scenario Documents (ESD), the Technical Guidance Document (TGD), the Technical Notes for Guidance (TNsG) and tools such as the European Union System for the Evaluation of Substances (EUSES).

ECT supports your company during the complete BPD registration process by providing the following services:

• Identification of the product type and specific information requirements
• Data mining, data gap analysis and literature research
• Data management, evaluation and reporting with the IUCLID 5 database software
• Placing, performing and monitoring of required studies according to Good Laboratory
• Practice (GLP)
• Conducting the environmental risk assessment and specifying exposure scenarios
• Dossier preparation: Doc III (A, B), II (A, B, C) and I
• Assessment of substances of very high concern (SVHC): CMR, PBT, vPvB, endocrine
• disruptors, equivalent level of concern
• Classification, Packaging & Labelling (CLP) according to the Globally Harmonised System
• (GHS) and EU requirements
• Communication with the competent authority (pre- and post submission)
• Project coordination and communication with all participants
• Submission of the dossier documents to the competent authorities