Programme

  1. Moderator: Dave Dillon, Senior Regulatory and Compliance Analyst, Chemical Watch, UK

  2. Session 1: Overviews

  3. Welcome and introduction

  4. EU Commission overview

  5. Echa overview

  6. Status update on working with the BPR – progress and challenges from a competent authority perspective

    • Finishing the review programme and renewal of active substances
    • Experiences with product evaluations of new product types
    • Challenges with biocidal products not yet under approval and treated articles
    • EU cooperation in a digital world
  7. Challenges and opportunities of the BPR from an industry perspective

  8. Q&A and panel discussion

  9. Networking and break

  10. Session 2: The product authorisation and active substance renewals processes

  11. Two years after guidance release – state of play and experiences with biocidal product families (BPF)

  12. Experiences with renewals for wood preservatives

  13. Case study: challenges for a small business under the BPR

  14. Recent additions to Annex I of the BPR: regulatory status and clarification on ‘natural’ substances

    • Definition of ‘natural’ substance
    • Food and feed and simplified authorisation for biocidal products
    • Essential oils and Article 28 compliance
    • Microorganism-based products
    • Take home messages
  15. Q&A and panel discussion

  16. Networking, break and Chemical Watch membership and platform demo 13.40-14.20

  17. Session 3: Early experiences in the start up and running of the post-Brexit biocides scheme in Great Britain (GB BPR)

  18. Authority experiences: authorisations and enforcement of the GB BPR

    • The legislative regime
    • What has not changed
    • What might change
    • Hot topics/future priorities
  19. GB BPR industry experiences so far and prospects for the future

    • Industry example of a PT9 biocide used in leather manufacturing
    • Preparations for Brexit, for example surveys of all global suppliers 
    • Transfer of Art 95 listing 
    • What we expect for future submissions
  20. Legal issues

    • Data rights
    • Strategic planning
    • Regulatory divergence
  21. Q&A and panel discussion

    Wayne Giordmaina, Regulatory Affairs & Project Manager, Biocides, knoell Korea Ltd, South-Korea, will be replaced during the live Q&A and panel discussion by his colleague 

  22. Networking and break

  23. Session 4: Overlaps and scope issues of the BPR with other legislation

  24. Preliminary ARTFood guidance for professional uses

  25. Comparison for food contact legislation and the BPR for PT4

  26. Q&A and panel discussion

  27. Take home messages

  28. End of day 1