On August 8, 2013, Gretchen Bowker, co-founder and COO of Pearl Pathways, will host a webinar on ComplianceOnline.com reviewing the similarities and differences in the regulatory paths and requirements for drugs, biologics and medical devices. It will discuss the applicable FDA “Centers,” the IDE and IND process, as well as 510k, PMA, NDA and BLA submission processes.

Where: ComplianceOnline.com: Register here.

Fee: $249.00

When: July 25, 2013

Duration: 60 minutes


For more information and registration click here.