Webinars >>FDA Approval
How to Apply for Emergency Use Authorizations (EUA) for Various FDA Regulated Products

The Emergency Use Authorization (EUA) authority permits FDA to assist strengthen the nation’s public health protections against CBRN threats by facilitating the supply and use of MCMs required throughout public health emergencies.
The webinar will help in determining your eligibility while applying for the EUA and will cover the following topics:
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  • The pre-EUA process
  • Diagnostics for a new disease
  • Drugs: new, repurposed and off-label use of approved drugs
  • Biologics: Vaccines, antibody and cellular therapies
  • Special release of products by FDA

​Who Should Attend:
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  • Supervisors, Managers in Operational Management and Regulatory affairs
  • Project management personnel
  • Senior management executives (CEO, COO, CFO, etc)
  • Manufacturing managers, supervisors & personnel
  • Crisis managers, disaster management and business continuity management personnel
  • People investing in FDA-regulated product development projects
Date: December 23, 2020
​Duration: 60 Minutes
​Time: 12 PM EST

Speaker: Mukesh Kumar
​PhD, RAC | Brij Strategic Consultations,  USA
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    For more info, fill the box below. We will contact you within 24 hrs.
For additional information on the workshop agenda and logistics, please call 410-501-5777 or email: info@fdamap.com