Federal Register Notice: FDA will hold a public workshop 9/18-19: “The Patient Preference Initiative: Incorporating Patient Preference Information into the Medical Device Regulatory Processes.” Participants will discuss ways to incorporate patient preferences on the benefit-risk tradeoffs of medical devices into the full spectrum of CDRH regulatory decision making. It also aims to advance the science of measuring treatment preferences of patients, caregivers, and health care providers. The workshop will be held from 8 a.m. to 5 p.m. at FDA’s White Oak Campus, 10903 New Hampshire Ave., Bldg. 31 Conference Center, Section A of the Great Room (Rm. 1503), Silver Spring, MD. Contact Nada Hanafi, (301) 796-5427. To view this notice, click here.