TSGE has extensive experience of the Biocidal Products Directive (98/8/EC). We have prepared and submitted dossiers for active substances in a range of product types. Following submission, TSGE is actively involved in liaising with the Rapporteur Member State and other regulatory agencies on behalf of our clients through the whole evaluation process providing a complete regulatory and scientific consultancy service up to inclusion onto Annex I of the Directive.
TSGE also offers a pan- European product registration service under the various transitional arrangements currently in place in the Member States prior to Annex I inclusion. Following Annex I inclusion we are able to assist in all aspects of product re-registration and with mutual recognition procedures.
Our highly experienced scientific consultants are able to provide all the necessary technical support to the registration process such as conducting completeness checks, preparing summary dossiers, human health and environmental risk assessment and efficacy evaluation.
TSGE is also actively involved in lobbying the EU Commission on data requirements and other issues and we have prepared various position papers and regularly attend the EU technical meetings.
If you would like any further information on our services, please do not hesitate to contact us.