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Life Sciences 101

Biologics: From Bench to Clinic


Description

In this module, Vice President of Biologics at Eurofins CDMO Alphora, Tariq Massad (Ph.D., PMP), delves into the process of developing and manufacturing monoclonal antibodies (mAbs). You will learn what a biologic is, how mAbs differ from other biologic product classes, and how mAbs move from the drug discovery stage through to formulation and filling.

Content
  • Introduction to Biologics
  • Introduction to Biologics
  • Assessment: Introduction to Biologics
  • Introduction to Monoclonal Antibodies
  • Introduction to Monoclonal Antibodies
  • Assessment: Introduction to Monoclonal Antibodies
  • The Monoclonal Antibody Production Cycle
  • The Monoclonal Antibody Production Cycle
  • Assessment: mAb Production Cycle
  • Manufacturing Monoclonal Antibodies: Quality by Design
  • Manufacturing Monoclonal Antibodies: Quality by Design
  • Assessment: Quality By Design
  • Manufacturing Monoclonal Antibodies: Technology Transfer and Process Validation
  • Manufacturing Monoclonal Antibodies: Technology Transfer and Process Validation
  • Assessment: Technology Transfer and Process Validation
  • Manufacturing Monoclonal Antibodies: The Upstream Process
  • Manufacturing Monoclonal Antibodies: The Upstream Process
  • Assessment: The Upstream Process
  • Manufacturing Monoclonal Antibodies: The Downstream Process
  • Manufacturing Monoclonal Antibodies: The Downstream Process
  • Assessment: The Downstream Process
  • Manufacturing Monoclonal Antibodies: Formulation and Filling
  • Manufacturing Monoclonal Antibodies: Formulation and Filling
  • Assessment: Formulation and Filling
  • Working in a GMP Environment
  • Working in a GMP Environment
  • Working in a GMP Environment
Completion rules
  • All units must be completed
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