Compliance
Cross-border trade in medical equipment is a regulated activity on both sides of the border. Our compliance framework protects our customers, our suppliers and ourselves.
EU regulatory provenance
Equipment supplied carries CE marking under the applicable EU framework (MDR 2017/745 / IVDR 2017/746 as relevant), sourced from manufacturers or authorised distribution channels with full technical documentation and declarations of conformity.
Export control & sanctions screening
Every transaction is screened before commitment: counterparty screening against applicable EU sanctions lists, end-user and end-use verification, and assessment of re-export risk. We do not engage in transactions designed to circumvent EU restrictive measures.
Documentation integrity
Commercial, transport and regulatory documentation is prepared consistently and retained — supporting customs clearance, registration procedures and any subsequent audit by manufacturers, banks or authorities.
Banking & payment transparency
Payments are routed through EU banking with transparent commercial documentation. We support letters of credit and documentary settlement where required by the transaction.