Bringing the details together
Import enquiries assessed around the product, source country, intended market and authorisations applicable to the proposed route.
Medicine imports
The requirements for a medicine import depend on the product, where it is sourced and the market in which it will be supplied. A commercial opportunity should therefore begin with accurate product and source information, rather than an assumption that every route is the same.
PharmaGlobe’s importing focus is to bring the relevant commercial and regulatory details into a clear enquiry. We welcome discussions with appropriately authorised manufacturers, wholesalers and healthcare purchasers. The licences and responsibilities relevant to a proposed route must be established before any import or supply can proceed.
A closer look
The starting point is a precise product description and a clear understanding of the source. Manufacturer information, product presentation and the intended market help define what further information needs to be reviewed.
Manufacturers and pharmaceutical wholesalers can contact us about potential supply relationships. Introduce your organisation, operating permissions and the products or markets you wish to discuss.
An import enquiry should identify the proposed route, handling needs and available documentation. Responsibilities, release requirements and any route-specific permissions must be understood before commercial commitments are made.
From enquiry to next steps
Share the product specification, supplier details and countries involved in the proposed transaction.
The applicable permissions, responsibilities and documentation must be confirmed for that particular enquiry.
Only a suitable, properly authorised route can move forward to an agreed commercial arrangement.
Useful answers
Requirements differ according to the product, source and route. Each enquiry must be considered individually; a country’s inclusion in an enquiry is not confirmation that supply is permitted.
No. The authorisation needed depends on the activity and route. Current licences and their scope must be checked for the proposed transaction.
Yes. Send your company information, relevant authorisations and a clear product list. An introduction does not constitute product approval or acceptance of a supply arrangement.
Start with your legal company name, source country, product list and relevant operating authorisations. Include the intended UK product presentation and the supporting documentation available for the proposed route.
An international product enquiry needs more than a medicine name. Strength, pharmaceutical form, pack size, labelling, source country and intended market help define what must be reviewed for a possible import.
Yes. Specify minimum remaining shelf life, storage conditions and expected arrival dates early. These requirements form part of the assessment of a proposed route and cannot be assumed from the initial enquiry alone.
Start a focused conversation with the PharmaGlobe trade team.
