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Website title: Drug and Biologic Contract Research Organization (CRO) | Medpace
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Rare disease clinical development is undergoing rapid transformation, driven by scientific innovation, evolving regulatory frameworks, and the need for more flexible, patient-centric trial designs. This webinar will explore the current rare disease clinical development landscape and the key trends shaping its future.
The webinar will highl...
Meet Dr. Sonia Quintas, MD, MSc, Medical Director
Medpace is proud to welcome Dr. Sonia Quintas, an accomplished and board-certified Neurologist, to our medical leadership team. Dr. Quintas brings nearly a decade of clinical and research experience across a broad spectrum of neurologic conditions, with deep specialized expertise in sleep disorders and headaches. ...
Ensuring cardiovascular safety is an integral component of the drug development process. Early detection of potential cardiac risks—such as lengthening of the QT interval and other ECG abnormalities—with increasing drug exposure is essential to protecting the safety of trial participants. Additionally, a well-executed Concentration-QTc (C-QTc) analysis
Meet Dr. Maxime Jeljeli, MD, PhD, Medical Director, Medpace
Medpace is pleased to announce the addition of a new immunology expert, Dr. Maxime Jeljeli, to the medical leadership team.
Dr. Jeljeli is a physician and scientist with over 13 years of combined clinical, academic, and pharmaceutical research experience in translational immunology....
Behind many successful clinical trials is a central laboratory partner that understands both the science and operational challenges faced by Sponsors, sites, and patients. At Medpace’s central labs, our strength lies in experienced lead...
