Join Compliance Services International (CSI) regulatory consultants Warren Scott and Stuart Green at Chemical Watch Biocides Symposium on 2-3 May, 2023 in Copenhagen, Denmark.
Stakeholder topics of interest this year include:
- Latest updates on European biocidal regulations;
- Regulatory processes and assessment updates in the European biocides sector;
- The assessment of endocrine disrupting chemicals under the BRP;
- Sustainability and the BPR;
- A panel discussion on how to increase public awareness of biocides in a blanced way;
- International updates
Warren and Stuart will be present throughout the event to meet with you and answer any questions you have regarding CSI’s regulatory and technical consultancy services. To contact them directly, please click the below “Contact Us” button to send an email.
Compliance Services International (CSI) is an award-winning consultancy providing innovative solutions to meet regulatory and environmental challenges. Regulatory requirements, environmental challenges, and global markets are ever-changing. Our diverse staff of regulatory professionals and scientists in North America and Europe, along with associates around the world, continually adapt to develop strategic approaches to meet our clients’ needs.
CSI has an established reputation in supporting registration of a range of biocidal/antimicrobial products including disinfectants, sterilizers, preservatives, and unique biocidal/antimicrobial applications. We support clients introducing their products in North America and European markets through cost-effective strategies.
In Europe, we assist with active substance approval and biocidal product authorizations to comply with the requirements for the European Economic Area (EEA) (i.e. EU27 plus Iceland, Liechtenstein and Norway). With the new GB BRP regulation now in force for Great Britain, CSI is able to offer GB Article 95 representative support for EU companies.
In the US, we help clients with US Environmental Protection Agency (EPA) and the Food and Drug Administration (FDA) regulated biocidal/antimicrobial products, label generation and amendments, as well as State registration management.
We also support the global marketplace and have successfully assisted firms with registrations in Canada, Latin America, Asia (China/Taiwan), Australasia, and other geographical markets.
Experienced Support For:
- Registration Dossier Preparation & Submission
- Regulatory Strategy
- Data Review & Evaluation
- Hazard, Exposure, & Risk Assessments for Human Health & Environment
- Task Force Management
- Litigation Support
- Endocrine Disruptors