Wednesday, April 23, 2014

Leap Ahead With EAP? FDA Proposes New Expedited PMA Pathway

Leap Ahead With EAP? FDA Proposes New Expedited PMA Pathway-thegraysheet: FDA’s newly proposed accelerated PMA program may have a long name, but the agency hopes it will significantly shorten the time to market for a select set of devices that target unmet needs for the most serious conditions. The “Expedited Access Premarket Approval Application for Unmet Medical Needs for Life Threatening or Irreversibly Debilitating Diseases or Conditions,” or EAP, was introduced today in a draft guidance (PDF), after CDRH signaled plans for the program earlier this year.