Advancing Aesthetics with Intelligence & Integrity

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Where Innovation Meets Growth

WeturnyourformulationsandlabbreakthroughsintoEU-ready,marketable,andprofitableproducts.

01

Doctors & Clinics

Innovation Sourcing, Brand Development, Website & Content

02

Brands & Distributors

Regulatory, Branding, Sales Ops

03

Manufacturers & Suppliers

Regulatory, Market Entry, Distribution

Built for Growth

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.

EU Market Entry

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.

Cosmetics Registration

CPNP Fast Track

Rapid Cosmetic Product Notification Portal registrations, claim audits, and CPSR safety reports completed in weeks.

Safety Assessment

CPSR

Full Cosmetic Product Safety Reports prepared by qualified safety assessors to meet EU Cosmetic Regulation (EC) 1223/2009.

Regulatory Affairs

RA Consulting

End-to-end regulatory affairs consulting for cosmetics, medical devices, and consumer goods entering the EU market.

MDR 2017/745 · IVDR 2017/746

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.

General Consumer Goods & Electronics

EU Responsible Person

Appointed EU Responsible Person (EURP) for general consumer goods and electronics requiring in-market representation.

Food Business Operator

Food Supplement Notification

EU notification and legal representation for food supplement brands entering European markets as a Food Business Operator.

Cosmetics Registration

CPNP Fast Track

Rapid Cosmetic Product Notification Portal registrations, claim audits, and CPSR safety reports completed in weeks.

Safety Assessment

CPSR

Full Cosmetic Product Safety Reports prepared by qualified safety assessors to meet EU Cosmetic Regulation (EC) 1223/2009.

Regulatory Affairs

RA Consulting

End-to-end regulatory affairs consulting for cosmetics, medical devices, and consumer goods entering the EU market.

MDR 2017/745 · IVDR 2017/746

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.

General Consumer Goods & Electronics

EU Responsible Person

Appointed EU Responsible Person (EURP) for general consumer goods and electronics requiring in-market representation.

Food Business Operator

Food Supplement Notification

EU notification and legal representation for food supplement brands entering European markets as a Food Business Operator.

Medical-Grade Labs

Innovation Sourcing

Direct sourcing of advanced actives, exosomes, and premium formulas from vetted medical-grade research laboratories.

Identity & Positioning

Brand Development

From clinical narrative to visual identity — we build brands that earn trust with European doctors, clinics, and consumers.

EU Channel Development

Distribution & Sales Ops

Access to verified distributor networks and end-to-end sales operations infrastructure built for European scale.

Go-to-Market

EU Market Entry Strategy

Structured market entry planning covering regulatory pathway, channel selection, pricing, and launch sequencing.

Web Design & SEO

Clinic Website Upgrade

Custom clinic websites and search-ready digital presence tailored to aesthetic practices and doctor-led brands.

Content & Social Automation

Clinic Content Autopilot

Repeatable clinic content workflows that turn doctor expertise into social assets with less production drag.

Medical-Grade Labs

Innovation Sourcing

Direct sourcing of advanced actives, exosomes, and premium formulas from vetted medical-grade research laboratories.

Identity & Positioning

Brand Development

From clinical narrative to visual identity — we build brands that earn trust with European doctors, clinics, and consumers.

EU Channel Development

Distribution & Sales Ops

Access to verified distributor networks and end-to-end sales operations infrastructure built for European scale.

Go-to-Market

EU Market Entry Strategy

Structured market entry planning covering regulatory pathway, channel selection, pricing, and launch sequencing.

Web Design & SEO

Clinic Website Upgrade

Custom clinic websites and search-ready digital presence tailored to aesthetic practices and doctor-led brands.

Content & Social Automation

Clinic Content Autopilot

Repeatable clinic content workflows that turn doctor expertise into social assets with less production drag.

What We Do

Tailored Solutions for Growth

Browse by who you are or what you need. Either way, you'll find exactly what applies to you.

CLINICSFOR AESTHETIC & MEDICAL CLINICS

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
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FOR AESTHETIC & MEDICAL CLINICS

Clinics & Doctors

CLINICS
AMVE — CLINICS & DOCTORS

Clinics & Doctors

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FOR COSMETIC & WELLNESS BRANDS

Brands & Distributors

BRANDS
AMVE — BRANDS & DISTRIBUTORS

Brands & Distributors

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FOR PRODUCERS TARGETING EU MARKETS

Manufacturers & Suppliers

MANUFACTURERS
AMVE — MANUFACTURERS & SUPPLIERS

Manufacturers & Suppliers

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COMPLIANCE & LEGAL REPRESENTATION

Regulatory Services

REGULATORY
AMVE — REGULATORY

Regulatory Services

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Inquire

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.

Global Headquarters

Europa Platz 2, 10557 Berlin

Germany

Corporate Inquiries

hello@amve.co

Berlin · Seoul · Singapore

Partnership Proposal

Ready for predictable, compliant market expansion? Submit your formulation and business details below.

Answer-engine overview

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.

Practical workflow

How the work usually starts

01

Clarify the route

AMVE first identifies whether the need is regulatory preparation, commercial entry, sourcing, private-label development, or a combined market-entry pathway.

02

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.

03

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.

FAQ

Common questions

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.