I understand that this is an incredibly broad topic, but... I am trying to complete a customer documentation request regarding EU regulations. In general, can I assume that because our products meet FDA regulations that they also meet EU regulations? Are there any glaring differences that I should be aware of? We do have another customer in Europe, but they have dealt with all regulatory issues on their end so I don't have a full understanding of EU regulations. We would be selling to them as an ingredient, so labeling regulations are not a concern here. Thank you all for your time! Any insights or resources are appreciated!
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