Cosmetic brands in United Arab Emirates must meet Luxembourg's specific regulatory requirements before placing products on the market. Ministry of Health enforces cosmetic safety regulations in Luxembourg, requiring Product Information Files (PIF), Cosmetic Product Safety Reports (CPSR), and registration through CPNP (Cosmetic Products Notification Portal).
Taylored Consultancy offers comprehensive cosmetic regulatory services for United Arab Emirates brands expanding to Luxembourg. Our expert team handles CPSR preparation, PIF compilation, product registration, labelling compliance, and Responsible Person services, ensuring your cosmetic products meet all regulatory obligations for successful market launch and sustained compliance.

From formula to finish—expert regulatory and quality support in
to get cosmetics from
United Arab Emirates
compliant, safe, and sale-ready in
Luxembourg
We assess your formulation against cosmetic regulations in
Luxembourg
to check for ingredient restrictions, safety concerns, and legal compliance.
We handle the
Ministry of Health
registrations, making sure your product is legally listed before it goes to market.
From supplier verification to compliance audits, we help brands protect their reputation by making sure every part of their supply chain meets safety and regulatory standards.
We work with qualified safety assessors to create your legally required Cosmetic Product Safety Report, ensuring full EU compliance for Luxembourg market entry.
Full management of your Cosmetic Products Notification Portal registration, ensuring accurate submission of all required information for the EU market.
Comprehensive label review ensuring INCI listings, warnings, and translations meet all Luxembourg requirements, preventing costly market rejections.
Understanding the regulatory landscape, competitor activity, and upcoming changes is key to staying ahead. We provide insight to help you make informed business decisions.
Complete Product Information File compilation and review service, covering all manufacturing details, safety data, and documentation required for Luxembourg compliance.
We act as your legally required EU Responsible Person, handling notifications, compliance documentation, and serving as your regulatory contact with Ministry of Health.
We arrange microbial, heavy metal, and stability testing, plus review marketing claims to ensure they're evidence-based and legally compliant for EU standards.
Regulatory compliance shouldn’t hold your business back. We take the stress out of the process, helping you get your products to market quickly, legally, and with confidence.

We’ve helped brands navigate competitor challenges, supported companies under MHRA scrutiny, and stepped in when businesses needed urgent regulatory intervention to stay on the market.
We’re known for helping innovative brands push boundaries, working with businesses launching cutting-edge, first-of-their-kind products that challenge the status quo.
Our expertise covers everything from Product Information Files (PIFs), UK Responsible Person (UKRP) and EU Authorised Representative (EC- REP) services, safety assessments, labelling compliance, and ongoing regulatory maintenance.
Whether you need a one-off consultation or long-term strategic support, we tailor our approach to fit your needs, timelines, and budgets.
Looking for a regulatory partner who understands business? Let’s talk.
Bethany has a wealth of experience in medical devices and is always providing a fantastic service. Having worked with Bethany on and off over the years I can safely say I would trust her regulatory advice. Thank you Taylored & the team!

We have been working with Bethany for 3 months now and are very impressed! She is super orgainsed, very knowledgable and does it all with a smile! Would highly recommend.
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Amazing! Went over and above working longer hours communicating with suppliers and getting all the relevant info. Quick to find solutions and overall very helpful. Thank you!
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