PSG-CASTL Biomanufacturing Regulatory Compliance Course

Overview

PSG-CASTL Biomanufacturing Regulatory Compliance helps experienced professionals deepen their understanding of GMP, validation, and product lifecycle expectations in regulated biopharmaceutical environments. Co-delivered with the Pharmaceutical Sciences Group, the course connects quality, manufacturing, and regulatory concepts in a way that supports more informed decision making across an organization.

What participants will learn

• Strengthen understanding of current GMP expectations within the Canadian biomanufacturing landscape

• Connect product lifecycle stages to manufacturing operations and quality outcomes

• Recognize why validation and quality issues are central to successful manufacturing

• Build broader understanding of regulated biotherapeutic development through to commercialization

• Apply a more proactive compliance mindset for day-to-day organizational decisions

Ideal audience: 

 Ideal for operators, supervisors, managers, MS&T teams, quality and validation personnel, scientists, engineers, and suppliers supporting regulated biopharmaceutical operations. 

Employer value: 

For employers, this course helps build stronger internal regulatory capability across functions that influence quality, compliance, and manufacturing performance.