content
Providing an overview of the rights and obligations in accordance with the minimum standard and the packaging law, with a focus on B2B industry to doctors, hospitals, laboratories, etc. Minimum standard of the packaging register of the central office; Classification of the various packaging materials in the different fractions. Difference between transport packaging and product packaging as well as between system participation and non-system participation. Definition of "end consumer" from the point of view of the central office.
We also look at the challenges that Extended Producer Responsibility (EPR) poses to companies with regard to their products and packaging. And finally, we give a brief overview of the manufacturer's labeling and licensing requirements, also with a view to Europe.
The focus of this event should cover both aspects - Regulatory Affairs Updates and MAH from a regulatory point of view - equally. The current regulatory trends and the requirements for obtaining the "Made in China" label and the associated localization requirements are presented.
topic overview
- What does the minimum standard regulate?
- System participation requirements – B2B and B2C
- Difference between transport and product packaging, packaging with special content
- When are you a “consumer”?
- What are the obligations of manufacturers of packaging that is not subject to system participation?
- Extended Producer Responsibility
- Labeling requirements for packaging - also outside of Germany
target group
All companies that deliver to larger end users such as doctor's offices, hospitals, laboratories,...
KONTAKT:
Online
