MedSource provides support for complex clinical trials with expertise in complex therapeutic areas such as oncology, neurology, and rare diseases and complicated study designs from first- in- human dose escalation to adaptive designed registration studies. As a company that supports the most complex clinical trials, we know they aren’t called trials for nothing. At MedSource, we know how to pivot to the demands of even the most challenging trial and how to support the needs of our biotech customers with flexibility and transparency throughout the study life cycle.
MedSource is an award-winning clinical research organization (CRO) that delivers high-quality clinical trials through strong relationships with specialization in oncology, neurology and rare diseases. We have participated in over 700 clinical trials globally; more than 200 of them have been in oncology. Our efforts support biopharmaceutical clients who conduct complex clinical trials in the most challenging disease states and patient populations. Our wide experience encompasses a range of therapeutic areas, product types, clinical trial phases and study designs. Whether a challenging therapeutic area or a sophisticated trial design, our highly experienced team excels at delivering results.
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"They played an integral part in not only the development of our over study plan, but specifically the development of essential documents: protocol, informed consent forms, case report forms, and a variety of study plans, specifically the monitoring plan and communication plan."