Product Registration & Notification Services
Some EU and UK Regulations require the registration of products that fall within their scope. The regulations covering medical products in particular, often require manufacturers to complete detailed and time-consuming registration processes before they can legally place their products on the market.
As an appointed Authorised Representative, Eurolink works to support its Clients through registration processes in whatever way they need. Our assistance may be limited to providing advice and guidance. However, when necessary, we can undertake the entire registration process on a Client’s behalf.
We can also support the process of obtaining any third-party product approvals that may be required before a product can legally be placed on the market in the EU or UK. We can work with EU Notified and UK Approved Bodies on behalf of our Clients to have products examined and the correct approvals issued ahead of registration or delivery to customers.
Our Product Registration and Notification Services include:
Providing advice on the registration requirements for different products, including Medical Devices, Chemicals and Cosmetics
Registering products with EU, UK and other national competent authorities
Updating compliance records in line with product development
Informing clients of changes to legislation and registration requirements
Management of 3rd Party Product Approval processes for the EU and the UK
Please be aware that these services are only available to Clients for whom Eurolink acts as an Authorised Representative in the EU and/or UK.