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Peachtree associates have vast experience in the comprehensive development lifecycle.


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Medical Device companies, especially those bringing their first product to market, face significant challenges. In recent years, regulatory authorities have become more demanding of the clinical proof of efficacy and safety. Healthcare cost containment and the Affordable Care Act create added pressure on new technologies to demonstrate clinical benefit over existing technologies.


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Our Clinical Operations team has significant experience in planning, implementing, and managing all phases of clinical trials in multiple therapeutic areas. When it comes to running clinical trials – from simple to complex multi-center global studies, our staff have seen more than most.


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Clinical Research Organizations grew out of the need to control the peaks and valleys of clinical development. Lulls in pipelines resulted in underutilization of highly-compensated internal clinical research professionals. CROs – that focus on the efficient conduct of clinical trials – could be utilized for a defined time to implement and conduct a specific trial.


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Having sat on your side of the desk, Peachtree was founded with the knowledge of what we wanted a CRO to deliver high quality, cost-effective services. To accomplish this, we invested in the development of our procedures and systems as a solid foundation for meeting the needs of our clients


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