Webinar On Managing Product Recalls in Accordance with Part 806
Sign up to be notified of new teleseminars daily! |
| Description: | It is inevitable that eventually a device manufacturer will need to execute a correction or market-withdraw for a medical device. The actual process of managing a market-withdraw is time consuming; and if poorly executed can result in a visit from the FDA, while alienating the customer base. It is not unusual for FDA to spend a fair amount of time reviewing the recall files during an inspection, especially if the device establishment has executed a Class I or Class II recall since their previous establishment inspection. 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 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=MD1441 |
| URL: | https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=MD1441 |
| Date: | Thursday, December 4, 2014 |
| Time: | 6:00pm-7:00pm UTC |
| Duration: | 1 hour |
| Access: | Public |
| Category: | Webinar* |
| Created by: | Public Access |
| Updated: | Friday, October 31, 2014 12:49pm UTC |
| : | $249 |
| : | 4169154458 |
| : | uttam@compliancetrainings.com |
| : | Uttam Mandal |
| : | 4169154458 |
| Comments: | None |