Agenda
- SESSION 4: Best practices for managing the BPR
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Tips and tricks for applicant on how to create a solid dossier
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Take aways from a competent authority (CA) seminar on best practice for national authorisations
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How to avoid pitfalls with mutual recognition and same biocidal products application
Karolina Pastuszko
Chief Specialist, The Office for Registration of Medicinal Products, Medical Devices and Biocidal Products -
Best practice for how to create a label, also avoiding the use of misleading terms
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Q&A
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Refreshment break
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Best practice on where to find relevant guidance
Jules Bossert, Sector Group Manager B4E, Cefic??
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How to avoid pitfalls with union authorisations
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How to avoid pitfalls for biocidal product families (BPF): Lessons learned so far with quat families
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Q&A
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Lunch and Networking
- SESSION 5: The latest testing an modelling updates
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How to assess biocides and residues in water treatment processes
Ursula Karges, Water Resource Management, IWW Water Centre??
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Substances of concern in BPF: Case studies
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'To bee or not to bee, that is the question!' New guidance on risk assessment for bees - impact on PT18 biocides
Naomi YoungManaging Consultant, Ramboll -
Q&A
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Refreshment break
- SESSION 6: Important efficacy considerations
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Efficacy data, from primitive to primordial
- How efficacy data influences many other aspects of a BPR product dossier??
- How to stay abreast of critical developments related to efficacy testing??
- How to increase acceptance of efficacy test results????
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Residual activity versus treated articles
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Q&A
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Close of conference