Product

Scope of Services

• The process of product registration in IMED and acquisition of the IRC code in support of import authorization,
• Review of documentation related to shipments ready for dispatch, with a focus on customs clearance requirements in the destination country,
• Identification of required quality and compliance testing based on product type and risk classification,
• Coordination of specialized testing, where required, through accredited European laboratories certified to ISO/IEC 17025,

Official representation on behalf of the client at international exhibitions and congresses, accompanied by experienced medical device specialists and engineers.