by Emily Sparrow | Aug 28, 2015
On September 10th, the second part of the Indiana Medical Device Manufacturers Council two-day program, REG 102, will be hosted. This program is designed to provide industry background and knowledge specific to FDA regulations to those who may be new to the industry...
by Emily Sparrow | Aug 28, 2015
As reported by Alexander Gaffney in RAPS in 2014, the Manhattan Institute of Policy Research (MIPR) claimed that the inconsistencies in review times at FDA were due to inefficiencies by the agency. Since then, FDA has argued that the variations at the Center for Drug...
by Emily Sparrow | Aug 28, 2015
Pearl Pathways is excited to announce the release of pharma, medical device, and new academic hospital case studies. This brings our total number of case studies to sixteen. Check out our dedicated case study website page here where you can learn through real life...
