Lisa (Treiber) Gallatin, RAC, VP of Regulatory Affairs and Technical Communication, Anisa Ahmed, Clinical Quality Specialist, and Robin Solinsky, VP of Technology and Innovation, had the opportunity to attend the FDA Town Hall with Dr. Michelle Tarver, Director of the Center for Devices and Radiological Health (CDRH), hosted by Medical Alley this week in Minnesota.
The event provided valuable perspectives on the future of medical device regulation and an important opportunity for the MedTech ecosystem to engage directly with FDA leadership.
As a specialized, device-focused CRO, Bright Research values opportunities like this to stay connected to evolving regulatory priorities, build strong relationships across the regulatory community, and continue supporting MedTech innovators navigating complex development pathways. These conversations are critical to helping ensure regulatory frameworks continue to support both innovation and public health.
Thank you to Medical Alley and the FDA for creating such an important forum for dialogue and collaboration.
#ResearchDoneBright #TeamBright #MedicalDevices #RegulatoryAffairs #ClinicalResearch #MedTech #FDA #MedicalAlley
