Webinar On Corrective and Preventative Action (CAPA) Throughout the Product Lifecycle
November 14, 2014 - Mississauga ON CACompliance Trainings
suzzane.d@compliancetrainings.com
Phone:4169154458
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. 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