Webinar On Managing Product Recalls in Accordance with Part 806
December 4, 2014 - Mississauga ON CACompliance Trainings
suzzane.d@compliancetrainings.com
Phone:4169154458
Device establishments that have a well-defined process for managing product recalls typically avoid many of the pitfalls associated with managing recalls in the fire-fighting mode. Granted, product recalls are challenging events, device establishments can benefit when recalls are efficiently and effectively executed. 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