Expert guides on MoCRA compliance, EU cosmetics regulation, ingredient safety, and global market entry. Everything you need to navigate cosmetic regulatory requirements.
Why European sunscreens use modern UV filters that are illegal in the US, what the FDA actually allows, and the regulatory reason for the gap — a reference guide for brands formulating sun care across markets.
Which cosmetic ingredients are banned or restricted in the US, EU, UK, and Canada — and why the same ingredient can be prohibited in one market and freely used in another. A reference guide for brand operators, with the key concentration limits and the regulations behind them.
A step-by-step walkthrough of submitting MoCRA-compliant facility registrations and product listings through the FDA's Electronic Submissions Gateway (ESG NextGen) — from FEI to acknowledgement.
Under MoCRA, serious adverse events from cosmetic products must be reported to FDA on MedWatch Form 3500A within 15 business days. Here's exactly what triggers the deadline, what to include, and how to submit.
Every cosmetic product placed on the EU market needs a Cosmetic Product Safety Report. Here's what goes into Parts A and B, who can write each part, and how to structure the document under EC 1223/2009 Annex I.
Everything cosmetics brands need to know about the Modernization of Cosmetics Regulation Act — facility registration, product listing, safety substantiation, adverse event reporting, and GMP requirements.
Complete guide to the EU Cosmetics Regulation — CPNP notifications, Product Information Files, safety assessments, ingredient restrictions, responsible person requirements, and labeling compliance.
The science behind cosmetic ingredient regulation — how SCCS, CIR, and FDA evaluate ingredient safety, set concentration limits, and determine what gets banned or restricted.
See how Cosmetica automates MoCRA, EU, and global compliance for your brand.