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:
For a full agenda and speakers click here.
This course has been pre-approved by RAPS as eligible for 10.25 credits towards a participant's recertification of their Regulatory Affairs Certification (RAC) upon full completion.