Every successful nasal care project connects a clear market need with the right formula, dispensing system and regulatory pathway. Neomedis brings these elements together with a team experienced in international healthcare markets.

ISO & MDR

Neomedis is ISO 13485 certified for medical devices and all products are CE compliant with MDR Certification.

GMP Sites

GMP Sites

All Neomedis products are manufactured in France, in GMP sites. Quality is our first priority.

Development

Development

Neomedis can adapt products specifically for your market using only natural ingredients.

Regulatory

Regulatory

Neomedis has a dedicated Regulatory team to provide you with all of the necessary documents for registration.

Support

Support

From marketing to logistics, Neomedis can help you get products to market quickly and efficiently.

Technology

Technology

Neomedis products use the latest pump technologies, delivery systems, and most sophisticated actuators.