Clinical Development

From managing your entire clinical program to conducting an individual clinical trial, our clinical teams can help you affordably design and operationalize your protocol and provide visibility into your studies.more

Medical Devices

Our device experts will help you navigate the increasingly complex global regulatory and clinical landscape in support of your PMA, 510(k), and CE mark application.more

Regulatory & Strategic Development

Whatever the scale or complexity, we have the breadth and depth of expertise to move your products from the lab to market while maximizing your success with regulatory authorities worldwide.more

Post-Approval & Registry

Once a product is approved for use, understanding its efficacy and safety profile can be challenging. Our post-approval specialists deliver integrated phase IV research and registry services designed for your epidemiology, health economic, and safety programs.more

As a digital clinical research organization (CRO), we combine the appropriate mix of experienced people, proven processes and technology that:

Optimized by our proprietary eClinical technology platform, TEMPO™, we are able to deliver on our solutions at up to a 30% savings compared to traditional service providers. 

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