AML Global Consulting helps manufacturers bring cosmetics, food supplements, medical devices, and specialty chemicals to market — across EU, FDA, and GCC regulations — without the delays and overhead of a large consultancy.
We manage EU, FDA, and ECHA submissions from start to finish — so your products get registered and your dossiers get approved.
02Reformulate, relabel, and comply across borders. We handle import requirements and market-specific adaptations for each target market.
04Safety Data Sheet authoring and quality system implementation — so your operations hold up under scrutiny.
You work with the specialists, not account managers. Every engagement is handled by regulatory scientists and chemists who know your regulatory framework inside out.
We run lean by design. Without the layers of a large consultancy, we move faster.
We hold active regulatory experience across the EU, US, GCC, and Asian markets — including territories most consultancies rarely cover.
<p>The updated notification portal goes live Q3 2026, affecting all cosmetic products containing nanomaterials. Companies must update submissions by September or face market withdrawal.</p>
<p>The CARES Act provisions are reshaping how over-the-counter drug products are regulated, with significant implications for ongoing reformulation projects.</p>
<p>ECHA has added five substances of very high concern to the candidate list, prompting urgent compliance reviews for fragrance and industrial chemical manufacturers.</p>
Tell us your product and target markets. We will identify your fastest, cleanest route to compliance — and start working on it immediately.