Hire industry experts to keep you ahead of the game
Navigating the complex world of FDA regulations can be overwhelming.
Navigating the complex world of FDA regulations can be overwhelming.
Barry Sugarman, is a former owner of a group of pharmaceutical, dietary supplement, device, and cosmetic manufacturing and distribution companies. Barry has over 20 years of experience at all levels with FDA regulated companies that are large, medium, and small. Barry is an expert in drug, biologic, device, combination product, dietary supplement, and cosmetic product development, regulatory affairs, and clinical trials.
Drive regulatory and commercial success for your drug, device, or combination product through a comprehensive strategic approach and development plan.
Ensure flawless interactions with regulatory agencies—from initial strategy, to submissions and meetings—informed by frequent interactions and up-to-date information.
Move your product efficiently and successfully through the clinic using a customized clinical trial design solution with an eye towards differentiated product labeling.
Avoid unnecessary delays and costs by integrating CMC components early in the development program, including strategic insights and management on vendors.
Reduce short- and long-term costs through a robust nonclinical program with support in methodology, strategy, study design and development.
Maximize the potential of your program throughout development and the commercial lifecycle with strategic insights that position your product for success.