What Do You Do UKALIA?

We operate as a support service mini enterprise and have streamlined consultancy-free, import and export regulatory matter for the medical devices and in-vitro diagnostic (IVD) sector. 

Manufacturers and suppliers intending to place medical devices or IVDs in the EU require an authorised representative, a service we provide. Similarly, entering the UK market requires a UK Responsible Person (UKRP), which we also provide.

For those exploring opportunities involving any items qualifying as quality medical devices or IVDs, along with distributors or importers interested in these products for the EU or UK markets, our team can assist with market access and registration. Commissions for you apply upon successful finalisation and product registration in the targeted markets.

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