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About MedPace

Medpace is a leading clinical research organization (CRO) that specializes in conducting global clinical research for the development of drugs and medical devices. With over 20 years of experience, Medpace has established itself as a trusted partner for pharmaceutical and biotech companies looking to bring new treatments to market.

At Medpace, the focus is on providing high-quality services that meet the needs of clients while adhering to strict regulatory standards. The company's team of experienced professionals includes physicians, scientists, and project managers who work together to design and execute clinical trials that generate reliable data.

One of the key strengths of Medpace is its ability to conduct trials across multiple geographies. The company has a global network of sites and partners that allows it to recruit patients from diverse populations around the world. This not only helps ensure that trial results are applicable across different regions but also enables faster patient recruitment and study completion.

Medpace offers a range of services throughout all phases of drug development, from preclinical studies through post-approval support. These services include protocol development, site selection and management, data management and analysis, medical writing, regulatory affairs support, pharmacovigilance monitoring, and more.

The company's expertise spans a wide range of therapeutic areas including oncology/hematology; cardiovascular/metabolic diseases; infectious diseases/vaccines; neurology/psychiatry; gastroenterology/hepatology; dermatology/plastic surgery/wound healing; ophthalmology/otolaryngology/allergy/respiratory diseases; women's health/fertility/endocrinology/reproductive medicine/pediatrics.

Medpace has built its reputation on delivering high-quality results with speed and efficiency. The company uses advanced technologies such as electronic data capture (EDC), interactive response technology (IRT), risk-based monitoring (RBM), adaptive trial design (ATD), biomarker analysis platforms among others which help streamline processes while maintaining quality standards.

In addition to its core business activities in clinical research services for pharmaceuticals/biotech companies worldwide - MedPace also provides consulting services related to regulatory compliance issues faced by these organizations globally including FDA regulations & guidelines etc., which makes it an ideal partner for those seeking guidance on navigating complex regulatory environments around the world.

Overall MedPace is an excellent choice for anyone looking for a CRO with extensive experience in conducting global clinical trials across various therapeutic areas using cutting-edge technologies while maintaining high-quality standards throughout all phases from preclinical studies through post-approval support.