Borderline Products and Borderline Issues: What Does It Mean?

Borderline products, which often blur the lines between categories like cosmetics, medical devices, medicines, and food supplements, pose unique regulatory challenges. New technologies add further complexity, making correct classification crucial for regulatory compliance. We specialize in guiding you through these complexities to ensure your products remain compliant whilst avoiding legal risks due to misclassification.

However, borderline products also present opportunities. By reclassifying a product, you may be able to make new claims, enhance its marketability, or access more favorable regulatory pathways. Our team works closely with you to explore these possibilities, helping you choose the best classification to maximize both compliance and commercial potential.

Regulatory strategy for Borderline Products

Our regulatory experts provide a strategic approach to classifying borderline products, ensuring you make informed decisions in a constantly evolving regulatory landscape. We analyze all available regulatory options and assess how each classification impacts your product’s claims and market potential. By carefully navigating the grey areas between product categories, we help you not only comply with regulations but also unlock new opportunities for growth, ensuring your product succeeds in the market.