By attending this webinar, you’ll gain very valuable insight into how CAPA systems work and function to satisfy user and patient requirements. You will gain insight on how your CAPA system works and ways to improve it. Perhaps the greatest benefit will be a better understanding of the quality system in ways that you can apply its principles throughout the product lifecycle for better design and risk control.
First, the CAPA total lifecycle (starting with defect discovery to final verification of root cause) will be discussed and analyzed. Then, starting with R&D, the product life cycles will be followed to show how the CAPA lifecycle changes and evolves throughout the product lifecycle stages and ways to use this data not only for defect prevention but also for more consistent production and product and process improvement. The final discussion covers the post-approval stage of the product lifecycle.
The webinar will include a PowerPoint presentation followed by a presentation of flowcharts that logically sequences the activities of the CAPA system.
Objectives of the Presentation:
Understand the importance of starting the CAPA system ASAP in the product lifecycle
Understand how the CAPA lifecycle changes from R&D to commercialization
Gain insight on how to make more effective use of the CAPA system
Areas Covered in the Session :
Introduction, Purpose, and Overview
Defining the quality system from R&D to product discontinuation
Brief review of the device and pharmaceutical lifecycles
Regulatory requirements and Guidance recommendations CAPA systems
Quality Principles that apply to CAPA systems
The CAPA lifecycle from defect discovery to file verification of defect cause (PowerPoint & flowchart)
The product lifecycle to Research and Development to Product Discontinuation (PowerPoint & flowchart)
Example of a CAPA procedure in flowchart format
Who Will Benefit:
Quality and Regulatory Affairs
Quality Control Laboratory
Senior Management
Management Representatives
Inter-functional departments such as
Production Department
Maintenance Department
Purchasing Department
Warehousing Department
Sales and Marketing Department
Purchasing Department
Price Tags:
Live
Single Live : For One Participant
$ 249
Corporate Live : For Max. 10 Participants
$ 899
Recording
Single REC : For One Participant - Unlimited Access for 6 Months
$ 299
For more information and enquiries contact us at
Compliance Trainings
5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Canada
Customer Support : #416-915-4458
Email : support@compliancetrainings.com
First, the CAPA total lifecycle (starting with defect discovery to final verification of root cause) will be discussed and analyzed. Then, starting with R&D, the product life cycles will be followed to show how the CAPA lifecycle changes and evolves throughout the product lifecycle stages and ways to use this data not only for defect prevention but also for more consistent production and product and process improvement. The final discussion covers the post-approval stage of the product lifecycle.
The webinar will include a PowerPoint presentation followed by a presentation of flowcharts that logically sequences the activities of the CAPA system.
Objectives of the Presentation:
Understand the importance of starting the CAPA system ASAP in the product lifecycle
Understand how the CAPA lifecycle changes from R&D to commercialization
Gain insight on how to make more effective use of the CAPA system
Areas Covered in the Session :
Introduction, Purpose, and Overview
Defining the quality system from R&D to product discontinuation
Brief review of the device and pharmaceutical lifecycles
Regulatory requirements and Guidance recommendations CAPA systems
Quality Principles that apply to CAPA systems
The CAPA lifecycle from defect discovery to file verification of defect cause (PowerPoint & flowchart)
The product lifecycle to Research and Development to Product Discontinuation (PowerPoint & flowchart)
Example of a CAPA procedure in flowchart format
Who Will Benefit:
Quality and Regulatory Affairs
Quality Control Laboratory
Senior Management
Management Representatives
Inter-functional departments such as
Production Department
Maintenance Department
Purchasing Department
Warehousing Department
Sales and Marketing Department
Purchasing Department
Price Tags:
Live
Single Live : For One Participant
$ 249
Corporate Live : For Max. 10 Participants
$ 899
Recording
Single REC : For One Participant - Unlimited Access for 6 Months
$ 299
For more information and enquiries contact us at
Compliance Trainings
5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Canada
Customer Support : #416-915-4458
Email : support@compliancetrainings.com
