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Substantiate the safety of all your cosmetic products and ensure that all your ingredients are safe and compliant with industry standards. With QSS Cosmetic Safety Substantiation solutions, you can demonstrate adequate substantiation of the safety of your cosmetic product by way of evidence provided by research, analyses, or other scientific evidence.
We help manufacturers or the responsible Person for a cosmetic product gather all the safety data related to cosmetic product ingredients from various robust sources such as valid scientific data and prepare a comprehensive report.
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Yes, cosmetic Safety Substantiation is mandatory. MoCRA requires all cosmetic products to undergo safety substantiation before being available for public use. This means manufacturers (or whoever’s responsible for the product) need to have documented proof that their cosmetics have been thoroughly tested and are safe for consumers.
Compliance with these regulations is essential to avoid legal issues, protect consumer safety, and uphold brand integrity. MoCRA defines “adequate substantiation” as any combination of tests, studies, research, or data analysis that a qualified scientific expert would consider sufficient to demonstrate, with a reasonable degree of certainty, that the cosmetic product is safe for use.
There isn’t a single prescribed method for safety substantiation. The approach varies based on factors such as the product’s ingredients, intended use, and potential risks. Common methods include:
Cosmetic product manufacturers, importers, or distributors are responsible for safety substantiation. They must ensure they have proper documentation to ensure the safety of their products.
Quality Smart Solutions provides comprehensive services that ensure your cosmetics meet all regulatory standards, giving you peace of mind and keeping your customers safe. Here’s how we help:
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Quality Smart Solutions is a global consulting firm, engaged in providing strategic support for products including NHPs, pharmaceuticals, and medical devices, in areas such as Regulatory Support, Site Licensing, Clinical Development and more.