With more than twenty years of industry expertise and an additional 20 years as a senior FDA investigator, Mr. Barreto has an outstanding depth of knowledge in quality and compliance. Drawing on his extensive background as an FDA investigator, he helps manufacturing organizations simplify redundant and complex activities that impact good performance practices and productivity. His extensive FDA experience and deep understanding of complex pharmaceutical processes and international GxP regulations enable Mr. Barreto to provide technical support for inspection readiness activities.

He gained valuable knowledge and expertise during his tenures at renowned international and multi-national companies, such as Teva Pharmaceuticals, Sanofi, and Janssen Pharmaceutica, where he held senior roles in quality and compliance at both the site and global levels.