MedSource is a full-service niche CRO specializing in oncology programs and other complex clinical trials. We have participated in more than 700 clinical trials globally; more than 200 of them have been in the area of oncology. Our efforts support biopharmaceutical clients who conduct complex trials in the most challenging disease states. Our wide experience encompasses a range of therapeutic areas, product types, clinical trial phases, and study designs.  

Through the years, our services have expanded to include clinical monitoring, clinical project management, regulatory affairs and submissions, QA auditing, study start-up services, feasibility and site selection, data management, biostatistics, safety reporting, and medical monitoring. Our goal is for our clients to return to MedSource when they need high-quality clinical trial support. It is our role to be a trusted advisor, making decisions and acting with our clients' best interests in mind.


Clinical trials, Pharmacovigilance, Medical writing, Regulatory Affairs





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