Are you looking to navigate the US FDA regulatory process for your company’s drug development journey? Join our webinar, where we’ll break down the essential steps to increase your company’s value and decrease your development timeline.

Date: 6th, October, 2024. 4 pm EET (6 am PST, 9 am EST)

Key Topics:
FDA Formal Meetings: When, Costs, and Your Options.
IND Submissions: The Five Modules, Time, and Costs.
Expedited Drug Development Programs: Fast Track, Priority Review, Breakthrough.

Hosted by Michael Barr, a seasoned chemical engineer with over 7 years of experience at SGS Nutrasource, who has guided clients through more than 200 IND submissions.

SGS Nutrasource is a global leader in clinical and regulatory affairs, working with esteemed clients like Harvard University. Company’s expertise spans oncology, rare diseases, cardiovascular diseases, med tech, and more.

Register by filling out a form HERE.