BEGIN:VCALENDAR
VERSION:2.0
PRODID:-//INNO HUB Lithuania//Events Calendar//EN
CALSCALE:GREGORIAN
METHOD:PUBLISH
BEGIN:VEVENT
UID:event-2019@innohublithuania.com
DTSTAMP:20260604T004625Z
DTSTART:20241006T130000Z
DTEND:20241006T140000Z
SUMMARY:Understanding the US FDA regulatory process
DESCRIPTION: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.\n\n\n\nDate: 6th\, October\, 2024. 4 pm EET (6 am PST\, 9 am EST)\n\n\n\nKey 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.\n\n\n\nRegister by filling out a form HERE.
LOCATION:Online
END:VEVENT
END:VCALENDAR