Agenda
**Note: timings are in CEST**
- Part 3: The product authorisation and active substance renewal processes
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Introduction
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Product authorisation processes: what is and is not possible
- Union Authorisation: The ironman amongst product authorisations?
- National Authorisation: One member state = fast lane?
- Biocidal Product Families: The option of having blue, green and yellow products?
- Single Product Authorisation: The hidden champion?
- COVID-19 impacts: Disinfectants, disinfectants, disinfectants!
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The renewal process including finalised criteria for full/limited renewals
- Explain Ctgb’s interpretation of principles of renewal of active substance approvals
- By guiding you through the general framework, including the latest criteria for limited/full renewals
- In order to collectively develop ‘fit for purpose’ renewals
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Exclusion and substitution in the context of active substances renewals
- BPR Article 5 exclusion criteria
- BPR Article 10 substitution criteria
- Active substances meeting exclusion/substitution criteria - public consultation
- Approaches to Art 5(2) derogation
- Consequences of meeting substitution criteria
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Q&A and panel session
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Break
- Part 4: Sustainable use, innovation and benefits of biocides under the BPR and biocides topics overlapping with other legislation
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Introduction
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Sustainable use from Member State perspective
- User categories
- Best practices and Integrated Pest Management
- Control of the use of biocides
- Compliance monitoring
- Additionally: Covid-19 and biocide registration
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Microorganisms under the BPR
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REACH, MDR and RoHS overlaps with the BPR
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Q&A and panel session
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Close of day two
