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From Proof-of-Concept through regulatory submission, Continental has Phase II-III and post market specialists who are able to advance every step of your clinical trials by every means possible. We are commited to making the approval process smooth, accelerated and controlled  growth in size and complexity of pivotal research trials

By providing world-class clinical teams experienced in managing complex Phase II and Phase III trials, Continental aids with reducing delays, errors, and costs. With our own quality control, we improve study efficiencies and increase process speeds while ensuring the accuracy of performance data

By providing world-class clinical teams experienced in managing complex Phase II and Phase III trials, Continental aids with reducing delays, errors, and costs. With our own quality control, we improve study efficiencies and increase process speeds while ensuring the accuracy of performance data

Additionally, because Continental has its own large and diverse patient database, we are uniquely situated to  help studies start up faster. Continental partners our network clinicians with top regulatory, patient recruitment, database design, medical writing, clinical logistics, and other experts throughout North America

The result is an optimized clinical process with minimized "dead air" between clinical trials and tactical use of integrated tools.  These tools that eliminate delays while securing patient safety, data collection, and efficacy results to satisfy regulators and stakeholders

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