Regulatory Affairs

MMC has extensive experience in all governmental regulatory affairs. Does your firm require a specific license to operate, to setup in a European country, we are here to assist.

We can provide an insight memo on what is required for your license application, clarifying the regulations and guidelines that need to be met, so that any inward investments done by your firm is well justified.

ensuring that products such as cosmetics, pharmaceuticals, wellness, novel-food and veterinary medicines meet legislative requirements, if your project requires property searching, design ideas, digital and social media engagement, even assist with meeting HR requirements for your project.

MMC Nordic focus on ensuring organizations are meeting all the applicable regulations, such as those established by the Food and Drug Administration, for products and services. Our specialists do so by completing and filing paperwork with the appropriate local, state, and EU authorities.

Get in touch today for further clarification with our Regulatory Affairs Director

E: director@mmcnordic.com

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