Agenda

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  1. Coffee

  2. Welcome and introduction by the moderator

    David Dillon David Dillon
    Independent Biocides Expert
  3. Session 5: Towards sustainability - authorisations, substitutions and regulatory adaption
  4. Competent Authority view on derogations - balancing risks and benefits

    • Criteria
    • Analysis of alternatives
    • Authority considerations
    Oliver Brylski Oliver Brylski
    Scientific Officer, BAuA
  5. Derogation case study: Biobor

    • Introduction to the Biobor derogations
    • The process and challenges
    • A strategy to full registration
    • Closing remarks: a short comparison between the EU and US regulations
    Patrick Eakins Patrick Eakins
    General Manager and Technical Director, Hammonds Fuel Additives, Inc.
  6. Antimicrobial resistance and biocides

    • Outline of antimicrobial usage and resistance monitoring in the EU
    • What’s needed to utilize this infrastructure for biocide resistance monitoring?
    • Which gaps will be filled by JPI AMR BIORESIST?
    Mike Brouwer Mike Brouwer
    Senior researcher, Wageningen Bioveterinary Research, Wageningen University
  7. Q&A session

  8. Refreshment break

  9. Sustainable use of insecticides

    • Regulatory framework
    • Challenges and solutions: how we navigate various obstacles to achieve our sustainability goals
    • Discuss current trends and developments: advancements in technology and changes in regulatory policies
    • Case studies and examples to illustrate real-world applications
    Yuhua Wu Yuhua Wu
    Sector group manager, Biocides for Europe, Cefic
  10. DU perspective: challenge of finding substitute insecticides that are approved for military systems

    • Difficulties in finding biocides in compliance with regulations deriving from:
      • military standards and specifications
      • aircraft/engine manufacturers
      • airworthiness authorities
    • Biocides that are effective against microorganisms/insects often causing corrosion on aircraft or are prohibited in the country where they are intended to be used
    Synne Enstrøm Synne Enstrøm
    Technical Manager Chemicals, Norwegian Defence Materiel Agency, Air System Division
  11. Q&A session

  12. Lunch and networking

  13. Session 6: Best practices for managing the BPR
  14. Product registrations, fees and enforcement of the BPR – perspective of the Irish CA

    VIRTUAL PRESENTATION

    • Register for both Article 89 transitional measures and authorised products
    • Fees associated with transitional measures, product authorisations and active substances
    • Lessons learned and the challenges faced through national authorization and the mutual recognition process
    • Some practices in the enforcement of the BPR 
    Mervyn Parr Mervyn Parr
    Agricultural Inspector, Pesticide Controls Division, Department of Agriculture, Food and the Marine, Ireland
  15. The Dutch strategic framework for biocides

    • Introduction to the Dutch strategic framework for biocides
    • Current developments in the EU
    • Opportunities for the REFIT of the BPR 
    Peter van Kampen Peter van Kampen
    Senior Policy Officer Biocides, Dutch Ministry of Infrastructure and Water Management
  16. Pros and cons of union authorisation versus national authorisation (via mutual recognition)

    • The requirements, as stipulated in the regulation 
    • SC Johnson’s experiences
    • Learnings and tips from experience 
    Andebet Kassa Andebet Kassa
    Associate Manager, Registration & Regulatory Compliance, SC Johnson
  17. Q&A session

  18. Refreshment break

  19. Session 7: Important testing and efficacy updates
  20. Efficacy-related updates

    • Active substance approval: sufficient to demonstrate an innate activity or is a full efficacy data package needed?
    • Special areas or uses, for example: air disinfection, insecticides against black flies, spiders, etc, where BPR guidance is scarce or missing for biocides 
    • Biocides and resistance 

     

    Darja Duh Darja Duh
    Efficacy Assessor of Active Substances and Biocidal Products, Chemicals Office of the Republic of Slovenia (CORS)
  21. The ECHA/EFSA guidance on drinking water treatment assessment in active substances and biocidal products dossiers

    • Applicability of the new guidance document
    • Overview of the assessment
    • Challenges and recommendations for dossier preparation
    Lydia Pape Lydia Pape
    Principal Scientist Environmental Fate & Exposure, Knoell
  22. Q&A session

  23. End of conference

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