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ID Week 2022!
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Since inception in 1992, Medpace has assembled a team of therapeutically focused physicians and professional staff who have extensive experience designing and conducing infectious disease clinical trials; this cross-functional team understands the issues from the perspective of the sponsor, the clinical investigator, the scientific leader, and the reviewer at regulatory agencies. Utilizing a one-stop approach to drug development, we keep your programs on course by combining efficient clinical trial management, comprehensive regulatory consulting, and innovative technologies to execute at the highest level.
With the Medpace Difference, you will also benefit from strong lab partnerships and a specialized Data Integrity Unit, who is dedicated to collaborating with the clinical team to ensure the protocol is maximally operationalized to collect appropriate microbiological, diagnostic and laboratory data to monitor protocol testing and identify trends or issues.
