Welcome to Qserve® America                                           

Qserve America, Inc., a member of the Qserve Group, is an independent consulting firm operating worldwide with extensive regulatory experience in the United States and Europe. Our office is located in Claremont, New Hampshire, just north of New York City.

Qserve America provides coordinated American and European strategic planning for both regulatory and quality needs, as well as guidance and implementation from design and development to market launch. Our services include all regulatory documentation and submissions for medical device companies worldwide. We have a wide range of clientele that include manufacturers of implantable devices, In Vitro Diagnostics (IVDs) and combination products.

With over two decades of experience in FDA regulated industry our goal is to guide and assist your organization in the most efficient and practical way to achieve registration and market approval. Timely product launch means more revenue sooner. Working with a company that understands the entire regulatory process and that can work with you every step of the way is the path to faster approval and market launch.

With Qserve America, you have a partner that will be here to help you today and in the future.

We invite you to browse the Qserve website to better understand the scope of our services. If you would like someone to contact you to discuss your particular needs, please click here!

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Qserve:  EUROPEAN AUTHORIZED REPRESENTATIVE Services  (EAR Services)