Dr. Murad Mohamed Al Saggaf has fair and practical experience in pharmaceutical facility design and project management for (plasma fractionation, recombinant proteins, Ceph, liquid, solid and injectables dosage form of pharmaceutical). He worked ( 2006-2009) as a part-time consultant and member of the committee for setting the guidelines for market authorization of Biosimilar recombinant proteins for Saudi FDA. He has 30 years experience in a pharmaceutical production environment and production management.
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