Regulatory updates, supplier data, reformulation, scientific monitoring… the key points manufacturers and toxicologists should review after the summer break.
Back to Toxicology: 7 Key checks for a strong start to september 2026 Read More »
Why has TPO, a key ingredient in gel nail products, been banned? Discover the toxicological and regulatory reasons behind the ban.
Gel Nail Ban: Why TPO Has Been Banned | Toxi Plan Read More »
Are Korean sunscreens really better than European sunscreens? Discover how the two regulatory systems compare in terms of UV filters, UVA protection, formulation, and cosmetic safety.
TPO in Gel Nail Products: A Toxicologist’s View on the UK Cosmetic Ban Read More »
Discover how the EU AI Act impacts medical devices and interacts with the MDR and IVDR, with insights from a toxicology and regulatory perspective.
The Impact of the AI Act on Medical Devices: Regulatory and Toxicological Considerations Read More »
Are Korean sunscreens really better than European sunscreens? Discover how the two regulatory systems compare in terms of UV filters, UVA protection, formulation, and cosmetic safety.
Nail Polish Safety: 2026 Recall & Toxicology Risks Read More »
Are Korean sunscreens really better than European sunscreens? Discover how the two regulatory systems compare in terms of UV filters, UVA protection, formulation, and cosmetic safety.
Korean Sunscreens vs European Sunscreens: What’s the Difference? Read More »
Discover the difference between cosmetic safety and efficacy. Learn how EU regulations, safety assessments, and cosmetic claims determine product performance.
Cosmetic Safety vs Efficacy: Why “Is This Product Good?” Is the Wrong Question Read More »
Discover the key differences between EU and U.S. cosmetic labeling requirements after MoCRA. Learn how INCI lists, allergens, colorants, and nanomaterials are regulated in each market.
EU vs U.S. Cosmetic Labeling Requirements After MoCRA | Key INCI List Differences Read More »
Créer un dossier réglementaire pour une matière première cosmétique est indispensable pour garantir sa conformité et permettre son utilisation par les marques.
Discover how material equivalence can help medical device manufacturers avoid unnecessary biocompatibility retesting, reduce costs and maintain regulatory compliance.
Material Equivalence: How to Avoid Repeating Biocompatibility Testing Read More »