The Food and Drug Administration (FDA) defines regulatory science as the science of developing new tools, standards, and approaches to assess the safety, effectiveness, quality, toxicity, public ...
This collaborative was convened to catalogue current efforts to advance the science of patient input, identify critical gaps in the knowledge base and other barriers that impede progress, prioritize ...
SPE/MPD MiniTec conference at MD&M West features medical polymer innovations, sustainability keynote, and device design ...
WEST LAFAYETTE, Ind.--(BUSINESS WIRE)--MED Institute, a leader in pre-clinical and clinical medical product development services, is proud to announce a strategic collaboration with Sus Clinicals, a ...
Academia converts research dollars into a variety of benefits that exemplify the return on investment. A continuous flow of graduates who contribute to industry goals upon earning a degree from their ...
The medical device industry remains a significant force in the global economy, with revenues exceeding $300 billion and a projected annual growth rate of 6%. The United States leads the market, ...
Team members with the U.S. Army Medical Materiel Development Activity (USAMMDA) joined some 30,000 attendees and exhibitors during the final day of the Association of the United States Army (AUSA) ...
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