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 ...

The Fast Company Impact Council is an invitation-only membership community of leaders, experts, executives, and entrepreneurs who share their insights with our audience. Members pay annual dues for ...

The U.S. Army Medical Research and Development Command released an updated version of its official product development book on January 3, 2020. The book, officially entitled the USAMRDC 2019 Medical ...

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) ...

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 ...

The term Secure Product Development Framework (SPDF) was introduced by FDA in the draft guidance "Cybersecurity in Medical Devices: Quality System Considerations and Content of Premarket Submissions" ...

Hoping to be both safer and quicker in moving ideas to products, the FDA released a "Strategic Plan for Regulatory Science," on August 17. The agency says it's a "sweeping modernization of the science ...