An Innovative Contract Research Organization Dedicated to Bringing Clinical Trials to Life

Dermatology

Together, Cu-Tech and Synteract create the leading dermatology CRO, with global capabilities and unparalleled access to sites and patients. Our focus on novel and required dermatology drugs provides dedicated research services unmatched in the market.
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General Medicine

As complexity of drug development increases, experience in one specialized area can help define strategic solutions in another. We leverage our breadth of experience in multiple areas with deep strength in focused indications to bring clinical trials to life.
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Neuroscience

Neuroscience-related disorders are some of the most confounding and complex to affect people. Our specialized experience in these trials aids you in developing treatments that improve functioning and help the lives of both patients and caregivers…
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Oncology

Like our clients, we are committed to the quest to cure cancer. But cancer is not just a single disease. It takes deep trial knowledge to know how to address its many forms. Learn how Synteract has stayed ahead of the trends leading towards new treatments…
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Pediatrics

Pediatric trials run the gamut of indications in drug development, but they all have primary things in common – working with children and their families requires specialized expertise and deep knowledge of regulatory requirements….
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Rare & Orphan Diseases

Rare and orphan diseases have unique characteristics, not the least of which is finding the right population for your trials. We know the investigators and study sites that can help to address your recruitment goals, among other challenges…
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5/12/2020 - 5/15/2020 : ASGCT 23rd Annual Meeting More...

2/20/2020: Synteract will host a webinar on “Assessing the Competition in Rare Disease Clinical Trials: The Need for a Thorough Feasibility Strategy” on Tuesday, March 10 at 8 a.m. PST/11 a.m. EST/4 p.m. BST/5 p.m. CEST. More...

3/10/2020: Identifying The Three Leading Ways Your ISS and ISE Can Derail Your Study - Compiling and submitting the ISS and ISE are a vital part of a successful new drug application submission to gain approval from the FDA.

Synteract Blog 

4/7/2020: Our guide breaks down the benefits of PK/PD modeling and simulation and how you can integrate these strategies to advance your next #pediatric study: http://ow.ly/v0Mb50z3YJ7

Synteract on LinkedIn

4/6/2020: Our study teams understand the complexities of infectious disease and vaccines trials, from accelerated patient enr… https://t.co/mQ1Ew5RgiG

Synteract Twitter Feed
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