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We Create Compliance for safer Markets
Your Consultant & Legal Representative in the EU, UK & Swiss Markets
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Representing non-EU based manufacturers in a successful EU Market entry safeguarding their future across the entire community.
Find your way through a complicated EU marketplace with the support of a professional.
For your products to legally enter the EU Market and continue to circulate, you must have valid documentation.
Ensuring compliance and registering products to be made available on the EU Market.
Representing non-EU based manufacturers in a successful EU Market entry and safeguarding their future across the entire community.
Safety of children’s products (excluding toys) – Draft Commission Decision
References to European standards complying with the general safety requirements of the
Food supplements in Italy: updates on the use of turmeric
On August 1, 2022, the Italian Ministry of Health published an update
MDR: Notice to Manufacturers for Implementation
According to Article 120 MDR 2017/745 medical devices that have obtained
EU Representation, EU product registration, Technical documentation review & submission, Eu Consultancy & Training.
Device registration, technical documentation, UK labels, MHRA registration, UKCA Mark
Swiss Authorized Representative, Technical Documentation, Product Registration, Swiss Consultancy, Legal & Training
Obelis International Offices are independent partners who are able to provide our clients with solutions offering the same level of expertise and professionalism in other global markets.
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We create compliance for safer markets & consumers.