Regulatory Affairs

Lexco has extensive experience in all governmental regulatory affairs. Does your firm require a specific license to operate, to setup in a European country, Lexco is 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.

Lexco ensures that products such as cosmetics, pharmaceuticals, and veterinary medicines meet legislative requirements, and even assist, from finding the necessary land, too meeting HR requirements for your project.

Lexco focus on ensuring organizations are meeting all of 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

Anne Teudt
RA Director
E: ateudt@interlexco.com

lexco-legal

Registered Office:
Sankt Peders Vej 6
DK-2900 Hellerup
Tel: +45 30 33 97 17
info@lexcodk.com