We select partners carefully. Our distribution relationships are long-term commitments, and we invest significantly in onboarding, regulatory support, and market development for each territory.
CCI REAGENT er medicinsk IVD-udstyr til selvtestning. Distribution kræver regulatorisk bevidsthed, operationel kapacitet og et reelt engagement i markedet. Vi leder ikke efter den største distributør — vi leder efter den rette.
The following criteria guide our partner selection process. Not every requirement needs to be met from day one, but we expect partners to demonstrate capability, intent, and a credible path to meeting these standards.
Established relationships with relevant procurement channels in your territory. This may include hospital procurement offices, pharmacy chains, laboratory networks, or wholesale distributors. We value depth of access over breadth of catalogue.
Erfaring med håndtering af IVD- eller CE-mærket medicinsk udstyr. Kendskab til lokale registreringskrav, forpligtelser til sikkerhedsindberetning og evnen til at understøtte overvågning efter markedsføring. Kendskab til IVDR er en stor fordel.
Warehousing capability with appropriate storage conditions. Order fulfilment systems capable of handling healthcare product logistics. Traceability systems for lot management and, where applicable, UDI compliance.
Willingness to invest in market development over a multi-year horizon. This includes dedicating sales resources, participating in training, and committing to agreed minimum order volumes. We seek partners who build categories, not those who list products.
The following baseline requirements apply to all distribution partnerships.
Note: These are baseline expectations. Specific terms are defined in the distribution agreement and may be adjusted based on territory, channel, and volume commitment.
If your organisation meets these criteria, we would welcome the opportunity to explore a partnership. The registration process is straightforward and confidential.
Registrer din interesse — vores partnerteam vil følge op med fuld produktdokumentation, regulatoriske filer og distributionsvilkår. Ingen forpligtelse. Fuld transparens.
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