Specializing in FDA Regulatory Matters

Next Upcoming Webinar: Navigating the FSVP Maze: A Primer for Customs Brokers and Importers – August 24, 2017

Nancy Chew

Independent Advisor, New Product Development and Submissions

Ms. Chew consults with a domestic and international client base on all matters pertaining to the development of new pharmaceutical and medical device applications from the development of data and studies to support the data through the regulatory enforcement after product approval. She helps prepares pharmaceutical toxicology analyses, licensing assessments, general management and strategic planning evaluations as well as regulatory research, and opinion. Her career has given her far reaching expertise in regulatory affairs and biomedical product development. She was one of two professionals who developed the regulatory affairs credential for RAPS, was elected as a RAPS fellow in 2009.

Nancy Chew - Senior Advisor for New Product Development and Submissions