Authorisation of Biocidal Products in the EU and More – Best Practice Steps to Navigate the Biocidal Products Regulation and Get Your Product to the Market


The web-Seminar will take place in 2 sessions of 3 hours each (9.00-12.00 h & 13.00-16.00 h CET) on the same day .


Your benefit

This web-Seminar will enable the participants to understand the procedures and timelines defined by Regulation (EU) No 528/2012, the Biocidal Products Regulation (BPR), for marketing and use of biocidal products in the European Union. The web-Seminar will explore the topic of treated articles and provide examples of products which are out of the scope of the BPR.

The web-Seminar is rich in practical examples and exercises, which ensure the participants both gain the knowledge needed but also can apply that essential BPR knowledge into real life registration examples and solve issues with the help of our experts.


  • Understanding the Biocidal Products Regulation (BPR)
  • Approval of active substances
  • Review programme – active substance/ product type combinations
  • Authorisation of biocidal products
  • Possible authorisation routes of biocidal products
  • The supply chain and the obligations of the stakeholders
  • How to correctly label a biocidal product
  • How to strategically plan submissions
  • BPR cost overview
  • Treated articles and borderline products
  • Current developments in the BPR: endocrine disruptors, in-situ systems, Brexit, COVID-19
Target audience: 
Regulatory managers and other key stakeholders (e.g. importers, distributors) in the supply chain looking for an introduction to the regulatory requirements of biocidal products and active substances as according to the EU BPR.
Language of training material: