2ND SESSION ADDED: Managing Deviations Under Health Canada GMP

***BACK BY POPULAR DEMAND - SECOND SESSION ADDED***

Join us for an in-person, advanced training session for intermediate to advanced pharmaceutical professionals. Gain practical skills to identify, investigate, and resolve deviations under Health Canada GMP regulations, with a focus on importer responsibilities.

Overview:

This hands-on training combines expert instruction, real-life case studies, and facilitated exercises to deepen your understanding of deviation management within the Canadian GMP framework. You will learn how to perform root cause analysis, implement effective CAPAs, and improve audit readiness, all with an emphasis on the unique challenges faced by drug importers under Health Canada regulations.

Attendees will learn how to:

• Recognize deviation types, their causes, and Health Canada’s regulatory expectations

• Investigate and document deviations effectively, including applying root cause analysis

• Implement best practices for CAPA and perform deviation trend analysis

• Strengthen your Quality Management System to align with Health Canada requirements

• Improve audit preparedness through effective deviation management and cross-functional collaboration

Lunch and light refreshments will be provided.