The Omnicon Group Blog August 2017 - Points to Remember with Your FDA Premarket Approval

New medical devices considered to be Class III must receive the Food and Drug Administration's (FDA) approval. This Class III approval, called Premarket Approval (PMA), is basically a license granted to the applicant to market devices that support or sustain human life, is of substantial importance in preventing impairment of human health, or presents a [...]The post August 2017 - Points to Remember with Your FDA Premarket Approval appeared first on The Omnicon Group.