Everything you should know on Simplified Authorisation

WEBINAR

February 12, 2025   |   11 a.m. CET   |   45 minutes 

Are you planning to place a biocidal product on the European market through a simplified authorisation (simplified BPR authorisation), but find the regulatory requirements, expected data, and national specificities complex? 

During this webinar, our experts will provide a clear and practical overview of the simplified authorisation framework to help you secure your regulatory strategy and anticipate timelines. 

In this webinar, our experts will cover the following topics: 

• Key regulatory principles: eligibility criteria for simplified authorisation and applicable legal framework 
• Required data: composition, classification, and justification of the “low-risk” criteria 
• Required tests
• Costs, timelines, and key milestones:  what to expect in practice when managing a simplified authorisation project 
• How EcoMundo supports you: from feasibility assessment to dossier submission, including regulatory strategy and coordination and analysis of tests 
  
  EcoMundo will provide you with a clear pragmatic and actionable perspective to help you determine whether simplified authorisation is the right pathway for your products - and how to manage it efficiently

 💡 We'll even have a Q&A session, so stay tuned.