Medmarc, Hyman Phelps & McNamara, and Virginia Tech have collaborated to assemble a group of esteemed speakers to deliver this two-day program that will explore the relationship between regulatory compliance and products liability.
Medical devices are regulated heavily by FDA─both before and after they are marketed. Manufacturers are also required to meet international standards. Failure to meet the challenges presented by these requirements exposes a company to a higher risk of products liability.
This conference will enhance your ability to meet these regulatory challenges and mitigate products liability risk.
Who Should Attend: