Webinar On Managing Product Recalls in Accordance with Part 806
December 4, 2014 - Mississauga ON CACompliance Trainings
uttam@compliancetrainings.com
Phone:4169154458
This Webinar breaks down the elements associated with the product recall process and provides attendees with a fundamental understanding of the FDA’s recall requirements delineated within Part 806, while providing the tools needed for compliance. Areas Covered in the Session : 21 CFR, Part 806 compliance requirements Understanding the different types of field actions: Market withdraw Stock recovery Correction Classification of Recalls Creating an effective Recall Packet The recall notification process Reporting recall-related activities to the FDA (required reports) Recovery and quarantine of product Disposition of recalled product (certified destruction or rework) Formal closeout of a recall, including the FDA notification process Who Will Benefit: Beneficiaries of this Webinar will be Quality Professionals Regulatory Professionals Customer Service Professionals And everyone involved in the recall process, including the customer notification process, FDA notification process; creation and issuance of recall packets; product recovery process; product quarantine process; management of 3rd-Party Recall Service Providers; and the destruction of recalled product. Price List: 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