Regulatory Services

Manufacturer Registration

CSSi LifeSciences is trusted by some of the world’s leading device manufacturers to successfully complete and manage all annual registration and regulatory requirements for medical device manufacturers operating in the U.S., and to facilitate the inclusion of approved devices on the FDA’s device listings website. CSSi LifeSciences also has the knowledge and expertise to serve as a U.S. Agent to represent your company’s interests before the FDA.

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