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Project Management &
           Protocol Development
Clinical Monitoring
Data Management & EDC
Medical Writing
Medical & Safety Monitoring
Quality Assurance

As the pharmaceutical industry continues the trend towards licensing-in of successful new formulations, an increasing number of smaller biopharma companies participate in clinical trials.

At Clinesian, our goal is to assist innovative drug and medical device companies with ancillary services such as data management, statistical analysis, and regulatory compliance in a collaborative and cost-efficient manner. We bring big pharma expertise (please see our Senior Staff bios) at the cost none of the other US-based CROs can match.

Many major pharmaceutical and biotechnology companies are our clients

The rate of outsourcing in early and late stage drug development is expected to fuel double-digit growth in the CRO business in the next 5 years, according to latest market research. At the same time, there is increased competitive pressure on CROs to provide high quality services at a lower cost.

List of clients available on request.







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