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Certified according to en iso 13485 - France

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PROGRESS SILICONES

France

PROGRESS SILICONES has been specialised in the manufacture of silicone parts and other elastomers for industry and the medical sector since 1985. PROGRESS SILICONES designs, manufactures and sells silicone parts for the most demanding industries. Sectors, such as: the food industry, nuclear power, cosmetics, aeronautics, pharmaceuticals and biomedical. From single parts to mass production, we create all types of moulded parts, overmoulding, extrusion, co-extrusion, manufacturing and cutting. All our production can be associated with specific marking and packing operations, according to your specifications. We are equipped with 2 Clean Rooms covering 550 m2 classed ISO 7 and ISO 8, adapted to the manufacture of medical and pharmaceutical products. Our quality management system is ISO 9001 and ISO 13485 certified.

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LOUISDERMA PARIS

France

Louisderma Paris ® was founded with the vision to keep motivating on skin and hair health by creating new and better types of treatments for physicians and patients. We work in close collaboration with the medical community to achieve this goal and have leading physicians on our advisory panel. Our technology is a game-changer in regenerative medicine like the IMD PLATELETE: a patient-friendly technology for rejuvenation of the skin. In recent years, Louisderma paris® has developed new meso cocktail products according to various skin and hair types through special technologies such as VIXOEYE, GAMACTIL, LINUTRX, CELLIO, and LINUGLO. Today, our products and technology are marketed in over 30 countries worldwide. We will continue to redefine the aesthetics landscape by pushing the boundaries through developing novel solutions in both cosmetology and medical device products and always we ensuring excellence in everything we do. LOUISDERMAP PARIS is committed to Quality and to consistently maintain the level of operations required to meet customer requirements. LOUISDERMAP PARIS’S products are manufactured under a Quality Management system which complies with the requirements of ISO 13485: 2016, iso 22716 and GMP Regulation. All medical devices are regulated and certified under the Medical Device Regulation, EU Quality Managment System Certificate- CE 0373.

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Certified according to en iso 13485 - France

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