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Tag: Regulatory Affairs

Clinical Development

[Webinar] The Complexities of Pediatric Rare Disease Trials: Regulatory and Operational Strategies for Success

  • January 25, 2022

In this on-demand webinar, Medpace experts share the operational and regulatory challenges associated with pediatric rare disease clinical trials.

Company Spotlight

Medpace Hires Seasoned Regulatory Strategist to Lead its Global Regulatory Affairs

  • June 29, 2021

With the addition of Dr. Caitilin Hamill, Medpace strengthens its ability to provide Sponsors guidance and support in all stages of their product development programs,…

Clinical Development

Partnership with Greenleaf Enhances Strategic Regulatory Affairs Capabilities

  • February 2, 2021

"This partnership strengthens our global Regulatory Affairs offering and allows us to expand our strategic capabilities to support our Sponsors’ programs.” - Jon Isaacsohn, MD,…

Clinical Development

Shortened Timelines for Regulatory Review by ANMAT Make Argentina an Excellent Choice for Clinical Research

  • July 27, 2017

Author: Wanda Dobrzanski M.D, Head of Clinical Operations Latin America, Medpace

On April 26th, The Ministry of Health in Argentina (ANMAT) issued a new regulation…