Regulatory readiness
We establish which registrations, declarations and technical documentation apply before committing to supply. Applicable frameworks are confirmed per product and destination market.
Quality & compliance
Requirements addressed before goods move
In medical and cosmetic trade, a shipment is only as good as its documentation. We treat compliance as part of sourcing, not an afterthought.
Requirements vary considerably by product classification and destination market. Rather than make general claims, we confirm the applicable framework for each specific product and market combination at the start of an enquiry.
Our approach
Four working principles
Supplier assessment
Manufacturers are reviewed for quality management practices, production consistency and their ability to supply batch documentation.
Quality control
Inspection scope is agreed with the client in advance and set out in writing before shipment.
Traceability
Batch and lot information is retained so any query after delivery can be traced back to source.
Documentation
What typically accompanies a shipment
- 01
Commercial documentation
Invoice, packing list and transport documents prepared for the route.
- 02
Product documentation
Technical and product information appropriate to the classification and destination market.
- 03
Origin & declarations
Origin evidence and any declarations required by the importing authority.
- 04
Batch records
Manufacturing batch or lot references retained for traceability.
This is a general outline. IMT does not publish certification identifiers or regulatory registrations on this website; verified documentation is provided directly to counterparties as part of a transaction.
Have a compliance question?
Send the product details and destination market, and we will confirm what applies before anything is quoted.