Gretchen Bowker (COO) and Diana Caldwell (CEO) at Pearl Pathways recently  presented at IMDMC’s 2018 Reg 101. The workshop took place on Tuesday, June 12, 2018 from 8am to 5pm at the Montage in Indianapolis, Indiana. The workshop was designed for regulatory professionals and lawyers in the medical device industry to give them insight into FDA regulations.

Diana was the moderator for the day and Gretchen led a discussion entitled “Pathways to Market- 510(K) Requirements”.

Product development pathways continue to evolve and become more complex. Pearl Pathways delivers seasoned, responsive consultants who can design global regulatory strategies to trim months and dollars off the product development path or expertly negotiate global health authorities’ interactions and filings. To learn more about our regulatory services click here.