Webinar On Corrective and Preventative Action (CAPA) Throughout the Product Life
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| Description: | This webinar will discuss how the CAPA system and associated processes such as design control, risk management, process control, and investigations can be utilized throughout the product lifecycle to address defect prevention. Both medical devices and pharmaceuticals will be included. 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 For more information about this event please visit https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=FDB1067 |
| URL: | https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=FDB1067 |
| Date: | Friday, November 14, 2014 |
| Time: | 6:00pm-7:30pm UTC |
| Duration: | 1 hour 30 minutes |
| Access: | Public |
| Category: | Webinar* |
| Created by: | Public Access |
| Updated: | Friday, October 31, 2014 12:44pm UTC |
| : | $249 |
| : | 4169154458 |
| : | uttam@compliancetrainings.com |
| : | Uttam Mandal |
| : | 4169154458 |
| Comments: | None |