The conference focused on the following topics:

  1. Update on the EU Guidance on Efficacy and challenges in the efficacy testing
  2. Annex VIII implementation and ECHA IT submission tools (including Unique formula identifier)
  3. Experience gained  so far with authorization / renewal  of biocidal products, in situ cases and ED
  4. Legal Aspects, data sharing

 Angelo by Vienna House Prague
Radlická 3216/1g
15000 Prague 5
Czech Republic

Dr. Edmund Plattner
Dr. Edmund Plattner
Independent consultant, Austria
Dr. Vera Ritz
Dr. Vera Ritz
German Federal Institute for Risk Assessment
Dr. Andrea Zikova
Dr. Andrea Zikova
German Federal Institute for Risk Assessment
Maria Luisa González Márquez
Maria Luisa González Márquez
Ministry of Health, Spain
Rafael Gozalbes
Rafael Gozalbes
ProtoQSAR SL, Spain
Maria Amon
Maria Amon
Federal Ministry for Sustainability and Tourism, Austria
Peter Kugel
Peter Kugel
VVGB Advocaten Brussels
Saulius MAJUS
Saulius MAJUS
Lithuanian National Public Health Centre
Dr. John Harrison
Dr. John Harrison
Syngenta Professional Solutions, Switzerland
Dr. Lonne Gerritsen
Dr. Lonne Gerritsen
Knoell Netherlands
Kristine Krafte
Kristine Krafte
Latvian Environment, Geology and Meteorology Centre
Daniele Ape
Daniele Ape
Scientific Officer – Dissemination and Processing Unit, ECHA
Katarzyna Szymankiewicz
Katarzyna Szymankiewicz
ECHA, Unit D2 – Biocidal Products

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