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LEVERAGING DIGITAL SOLUTIONS FOR
REGULATORY COMPLIANCE IN BIOMANUFACTURING
REGULATORY COMPLIANCE IN BIOMANUFACTURING
Date: March 21, 2024
Time: 12 Noon EDT
Time: 12 Noon EDT
Location: ZOOM
Duration: 1 Hour
On-demand webinar recording
The regulatory demands of advanced therapeutics manufacturing differ significantly from conventional pharmaceutical manufacturing. With the ever-increasing focus on patient safety and product quality by the FDA, it is imperative that biomanufacturers embrace digital solutions to comply with regulations and avoid warning letters.
Join Honeywell to learn more from Dr. Arshad Azwad on how biomanufacturing companies are leveraging digital systems to navigate these challenges.
- Common regulatory pitfalls at biomanufacturing sites identified by the FDA
- Digital solutions including EBR, MES, QMS, ERP, and LIMS to address regulatory pressure
- Holistic approach to biomanufacturing digital strategy
Arshad Azwad
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Arshad Azwad
Biomanufacturing Specialist
Speaker Bio: Arshad Azwad, Ph.D., is the Biomanufacturing Specialist for the Life Sciences vertical within Honeywell Process Solutions, responsible for identifying customer pain points and providing tailored solutions for different types of modality manufacturing (ranging from small molecule to cell & gene therapy). Arshad holds a PhD in Biopharmaceutical Technology from the National University of Singapore and an MBA from Cornell University.
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