Process Validation for Biopharmaceutical Manufacturing

Process Validation for Biopharmaceutical Manufacturing

This course reviews the regulatory requirements and methods for validating pharmaceutical and biopharmaceutical manufacturing processes. Topics covered, include: The history of Process Validation; Risk based analysis; QbD (Quality by Design); PAT (Process Analytical Technology); DOE (Design of Experiments); Process optimization and characterization.

Date(s): 11/06/2014
Day(s): Thursday
Class Time: 8:00 AM to 5:00 PM
Location: Capstone Center at Raleigh
Building: BTEC Room: 124
Instructor: Mark Witcher
Course ID:
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Tuition: $70

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