Advancing Aesthetics with Intelligence & Integrity
WeturnyourformulationsandlabbreakthroughsintoEU-ready,marketable,andprofitableproducts.
Doctors & Clinics
Innovation Sourcing, Brand Development, Website & Content
Brands & Distributors
Regulatory, Branding, Sales Ops
Manufacturers & Suppliers
Regulatory, Market Entry, Distribution
Regulatory clarity. Brand authority. Operational scale.
Whether you’re entering Europe, expanding your brand, or building a compliant supply chain — we bring together the regulatory expertise, marketing intelligence, and sales infrastructure to make it happen.
From lab to shelf — every step, handled.
Compliance, registration, sourcing, distribution. The disciplines that turn a great formula into a product Europeans can actually buy.
CPNP Fast Track
Rapid Cosmetic Product Notification Portal registrations, claim audits, and CPSR safety reports completed in weeks.
CPSR
Full Cosmetic Product Safety Reports prepared by qualified safety assessors to meet EU Cosmetic Regulation (EC) 1223/2009.
RA Consulting
End-to-end regulatory affairs consulting for cosmetics, medical devices, and consumer goods entering the EU market.
CE & EC REP — Class I MD & Class A IVD
Authorised EU Representative services for Class I Medical Devices and Class A In Vitro Diagnostics under MDR and IVDR.
EU Responsible Person
Appointed EU Responsible Person (EURP) for general consumer goods and electronics requiring in-market representation.
Food Supplement Notification
EU notification and legal representation for food supplement brands entering European markets as a Food Business Operator.
CPNP Fast Track
Rapid Cosmetic Product Notification Portal registrations, claim audits, and CPSR safety reports completed in weeks.
CPSR
Full Cosmetic Product Safety Reports prepared by qualified safety assessors to meet EU Cosmetic Regulation (EC) 1223/2009.
RA Consulting
End-to-end regulatory affairs consulting for cosmetics, medical devices, and consumer goods entering the EU market.
CE & EC REP — Class I MD & Class A IVD
Authorised EU Representative services for Class I Medical Devices and Class A In Vitro Diagnostics under MDR and IVDR.
EU Responsible Person
Appointed EU Responsible Person (EURP) for general consumer goods and electronics requiring in-market representation.
Food Supplement Notification
EU notification and legal representation for food supplement brands entering European markets as a Food Business Operator.
Innovation Sourcing
Direct sourcing of advanced actives, exosomes, and premium formulas from vetted medical-grade research laboratories.
Brand Development
From clinical narrative to visual identity — we build brands that earn trust with European doctors, clinics, and consumers.
Distribution & Sales Ops
Access to verified distributor networks and end-to-end sales operations infrastructure built for European scale.
EU Market Entry Strategy
Structured market entry planning covering regulatory pathway, channel selection, pricing, and launch sequencing.
Clinic Website Upgrade
Custom clinic websites and search-ready digital presence tailored to aesthetic practices and doctor-led brands.
Clinic Content Autopilot
Repeatable clinic content workflows that turn doctor expertise into social assets with less production drag.
Innovation Sourcing
Direct sourcing of advanced actives, exosomes, and premium formulas from vetted medical-grade research laboratories.
Brand Development
From clinical narrative to visual identity — we build brands that earn trust with European doctors, clinics, and consumers.
Distribution & Sales Ops
Access to verified distributor networks and end-to-end sales operations infrastructure built for European scale.
EU Market Entry Strategy
Structured market entry planning covering regulatory pathway, channel selection, pricing, and launch sequencing.
Clinic Website Upgrade
Custom clinic websites and search-ready digital presence tailored to aesthetic practices and doctor-led brands.
Clinic Content Autopilot
Repeatable clinic content workflows that turn doctor expertise into social assets with less production drag.
Tailored Solutions for Growth
Browse by who you are or what you need. Either way, you'll find exactly what applies to you.
Clinics & Doctors
You're building a practice that patients trust. We help you source the right products, build a brand that reflects your clinical standard, and get found online — so your reputation works for you beyond the treatment room.
- Innovation sourcing & white-label brand development for in-clinic exclusives
- Web design and SEO built for medical aesthetics and cosmetic practices
- Social media content automation — consistent, compliant, on-brand
Growth starts with a single conversation.
Whether you’re scaling a brand, launching a new line, or entering Europe for the first time — we’ll help you build it right from day one.
Europa Platz 2, 10557 Berlin
Germany
hello@amve.co
Berlin · Seoul · Singapore
What does AMVE do?
AMVE supports aesthetic medicine, medical skincare, cosmetics, and MedTech-adjacent companies with European market entry, compliance preparation, positioning, sourcing, distribution, and private-label skincare work. AMVE is most relevant when a product, clinic concept, or manufacturer needs to connect regulatory readiness with commercial execution in Europe.
Who AMVE serves+
AMVE works with non-EU manufacturers, cosmetic brands, laboratories, distributors, aesthetic clinics, doctors, dermatologists, and medical skincare partners. The common thread is a need to translate a product or concept into a credible European market pathway.
- Non-EU MedTech and aesthetic medicine manufacturers planning European expansion
- Cosmetic brands and laboratories preparing CPNP, CPSR, claims, and market-entry work
- Clinics and doctors building private-label skincare or sourcing innovation
- Distributors assessing whether a supplier is compliance-ready and commercially usable
How AMVE connects compliance and commercial work+
AMVE treats compliance, positioning, and distribution as connected workstreams. A product may need CPSR coordination, CPNP preparation, label or claim review, partner selection, sales materials, and a clear clinic-facing story before it is ready for the European market. AMVE supports that preparation and coordination without presenting itself as a regulator or approval authority.
What market translation means+
Market translation means turning technical formulation, device, or ingredient information into language, proof assets, and sales narratives that European clinics, doctors, distributors, and buyers can evaluate. It is not only translation between languages. It is the conversion of scientific and supplier-side information into commercially usable European context.
How does the work usually start?+
- Clarify the route. AMVE first identifies whether the need is regulatory preparation, commercial entry, sourcing, private-label development, or a combined market-entry pathway.
- Check readiness. The next step is to review available documents, product information, claims, positioning, and partner requirements so gaps are visible before outreach or launch work begins.
- Build the pathway. AMVE then helps structure the practical next steps, from CPNP or CPSR coordination to brand assets, distributor conversations, clinic concepts, and sales-support systems.
What does AMVE do?+
AMVE helps aesthetic medicine, cosmetics, medical skincare, and MedTech companies enter or grow in Europe by connecting compliance preparation, positioning, sourcing, distribution, and clinic-facing commercial execution.
Who is AMVE for?+
AMVE is for non-EU manufacturers, cosmetic brands, laboratories, distributors, aesthetic clinics, doctors, and medical skincare partners that need a practical European market-entry or growth pathway.
What does dual compliance mean at AMVE?+
Dual compliance means AMVE understands both cosmetic compliance topics such as CPNP, CPSR, claims, and ingredient review and medical-device-adjacent market-entry topics such as MDR readiness, CE positioning, representative coordination, and post-market support.
Does AMVE guarantee regulatory approval or market success?+
No. AMVE supports preparation, coordination, positioning, and commercial execution. It does not act as a regulator, notified body, or authority, and it does not guarantee approvals or commercial outcomes.