6-7 September 2017 – Nice Acropolis Convention Centre, Nice, France
TEAM mastery takes part in the CIR!
An opportunity to meet and get to know each other in person. We look forward to discussing and exchanging ideas on the latest regulatory updates, potential issues, and solutions.
SAVE THE DATE: Thursday, 7 September 2017 11:35 – 12:05
Monica Locatelli presents a talk on Exposure Scenarios: “Exposure Scenarios: communication along the supply chain, scenarios for mixtures”
- Regulatory obligations on mixture scenarios
- Challenges
- Possible solutions: top-down and bottom-up
- Practical examples
CIR IN NICE – Meeting point for leading companies in the chemical and agrochemical sectors
The CIR fair positions itself as a meeting point for professionals in regulation, registration, human health, toxicology and product stewardship working across various chemical industry sectors, aiming to create new business opportunities. Moreover, it is also a place for discussion on the latest regulatory updates and their implications.
Once again, CIR is a networking opportunity linking industry and policy makers to discuss and develop better regulatory strategies for chemicals, biocides, and agrochemical products.
Bringing together more than 400 REACH consultants, laboratories, regulatory experts, toxicologists, ecotoxicologists and many others to exchange on the latest regulatory and technological developments on agrochemical products, biopesticides, REACH and BPR regulations.
MAIN TOPICS
Improving communication and management along the supply chain
• Interactive workshop on best practices for risk and product management
• Improve communication channels along the supply chain to ensure compliance and assess new REACH obligations
• Explore practical strategies for managing SVHC across the supply chain
• Cost reduction strategies: how to achieve them without risking compliance?
Evaluating technical and commercial strategies for REACH compliance
• SVHC: how is F. Hoffmann-La Roche dealing with the increasing number of SVHCs?
• Get a crucial update on the 2020 roadmap and assess the impact of the authorization process on the industry
• Examine the practice of data sharing and assess how to improve the process; Clariant’s experience
• Strategies to ensure the quality of safety data sheets: clarify what should be included according to requirements in different countries
Preparing for the 2018 deadline
• ECHA feedback on the 2018 deadline: what happens if companies fail to meet the registration requirements on time?
• Guidance from competent authorities: examining how they can support SMEs in preparing for the deadline
• Industry case studies: how companies are preparing and what the impacts are
• Direct responses from the UK, Austria, and Italy on the application of REACH regulation in member states
CONTACTS
Website: https://lifesciences.knect365.com/cir/
VENUE
1 Esplanade Kennedy – BP 4083 – 06302 NICE CEDEX 4
Tel: +33(0)4 93 92 83 00
Email: dcom@nice-acropolis.com
Website: http://www.sean-acropolis.com/