Overview
Expanding into new markets requires local regulatory knowledge, trustworthy distribution partners and a supply chain that protects your product and brand. We provide all three – as a wholesaler that buys and supplies your products, and as a consultancy that manages registrations and market entry.
We work with originator companies, generic manufacturers, consumer health brands and medical device producers that hold GMP, ISO 13485 or equivalent certification.
What you gain
Market access
Entry into multiple markets through one partner with regional knowledge.
Registration management
Dossier adaptation, submissions and lifecycle maintenance handled for you.
Brand protection
Documented, GDP-aligned distribution that keeps your product out of grey channels.
Tender participation
Positioning of your products in public and institutional procurement.
Commercial clarity
Transparent pricing structures and regular market feedback.
Reduced complexity
One contract, one contact, multiple countries.
What we look for
- Valid GMP (WHO, EU, PIC/S) or ISO 13485 certification
- Products with CTD-format dossiers or technical files suitable for registration
- Willingness to support registration with samples and documentation
- Stable manufacturing capacity and supply continuity
- Commitment to pharmacovigilance and quality cooperation
How to start
- 1
Introduction
Share your product list, certifications and target markets with us.
- 2
Assessment
We evaluate market fit and registration pathways and propose a cooperation model.
- 3
Agreement
Distribution, consultancy or combined agreement with clear responsibilities.
- 4
Execution
Registration, first orders and ongoing market development.