MedSource Clinical Monitoring Services

MedSource is a leading niche CRO providing reliable service delivery, project specific therapeutic experience, and involved senior management to our customers. Through our offices in North America and our affiliates in South America, we have earned the confidence of the pharmaceutical and biotechnical industries by participating in over 400 clinical studies.

Over the past decade we have built a sound reputation as a solution provider - offering a broad range of support services throughout every phase of clinical testing. We have extensive experience with Phase I-IV studies across most therapeutic areas but offer particular expertise in oncology, infectious disease, and CNS trials.

• Project Management
  Our project managers are responsible for the overall conduct of a clinical study and rely on proven, real world management skills to achieve success.
• Clinical Monitoring
  We offer one of the finest clinical monitoring teams in the industry to ensure protocol and regulatory compliance as well as timely submission of high-quality data.
• Regulatory Affairs Management
  Our regulatory affairs department is comprised of a diverse group of highly trained and knowledgeable professionals.
• Other Support Services
  MedSource is pleased to offer additional support services through our partners.