Mohammed Sanad is a Regulatory Affairs Manager at Baxter, where they leverage over 10 years of regulatory affairs experience to oversee complex global regulatory submissions across various therapeutic areas, including biologics and oncology. With a proven track record in both early and full development programs, they have successfully managed submissions for new drug applications and marketing authorizations. Previously, they worked as an Authorized Regulatory Product Specialist at Zimmo Trading Establishment from 2004 to 2011. Mohammed's expertise encompasses CMC regulatory affairs, regulatory strategy, and compliance, driving collaboration with teams and health authorities to meet regulatory standards.
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