This webinar will provide a clear overview of the regulatory processes required to add a substance to positive lists under EFSA (EU 10/2011regulations) and BfR (Germany) recommendations.

Understanding the eligibility criteria and regulatory requirements is essential for a successful submission. We will explore the role of each authority in substance evaluation and explain the key steps involved in preparing and submitting an application. The discussion will also cover best practices to optimize approval chances and accelerate market entry.

This session is designed for professionals in the food contact materials industry who want to stay ahead of regulatory developments and ensure compliance with international standards.

30 April 2025 | 8am EDT, 12pm GMT, 2pm CEST

By completing this form, you submit your information to the webinar organizer, who will use it to communicate with you regarding this event and their other services.