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Agenda
Requirements for market authorisation under the BPR
The trainers will take you through the requirements for approval of biocidal products under the BPR that will enable you to distinguish between the pros and cons of the different application procedures.
Michael Fink, DHI, Denmark; Jack Frausing Nielsen, DHI, Denmark
Refreshment break
Data and documentation requirements
The trainers will take you through the mandatory elements for an application, including data and documentation requirements and you will learn how to structure the application process.
Lunch
The biocidal product family concept
Legal requirements for endocrine disruptors
Refreshment break
IT Tools
Instructions on how to use the R4BP 3 (Register for Biocidal Products), IUCLID 6 and SPC Editor programmes. You will also be briefed about the upcoming SPC IUCLID format.
BPR status
The instructors wrap-up the course with an overview of the status of biocide legislation at national and EU level.