Expertise
Authorized Representation
We support non-resident manufacturers with authorized representation requirements that form part of their regulatory activities in Ukraine.
Why Representation Matters
Depending on the product and applicable regulatory framework, a non-resident manufacturer may need an authorized representative in Ukraine to fulfil specific regulatory responsibilities. Representation therefore needs to be considered as part of the wider compliance structure rather than as an isolated administrative step.
When It Becomes Relevant
The need for authorized representation depends on the product, the applicable legislation and the responsibilities assigned to the manufacturer. Establishing this requirement early helps integrate representation into the overall regulatory pathway.
Our Role
We coordinate authorized representation requirements within broader regulatory projects, helping align responsibilities, documentation and communication with the applicable regulatory framework.
Typical Coordination Activities
Regulatory Assessment
Reviewing the product context and identifying whether authorized representation forms part of the applicable regulatory pathway.
Representation Coordination
Coordinating the representation arrangement and its connection with the wider regulatory project.
Documentation
Helping organise documentation and information relevant to the responsibilities of the manufacturer and representative.
Ongoing Coordination
Maintaining communication and alignment as the broader certification or market access project progresses.
Questions or requests are welcome.
Let's discuss your context
Share the key details of your question, product or regulatory situation. We can then establish the relevant context and consider the practical next steps.