‘Product Recalls Series’ Returns to Indy

Second annual event brings together key stakeholders

Published: Wednesday, March 27, 2013 - 12:34

(CBI: Woburn, MA) -- For the past eight years, CBI’s Product Recalls Series has led the way in providing key updates and best practices for successful execution of drug, device, and diagnostic recalls corrections.

CBI’s Annual Product Recalls Summit, being held in Indianapolis on June 11–12, 2013, will unite all stakeholder voices, including manufacturer, regulatory, hospital, wholesaler, and distributor, to help increase compliance and efficiency when encountering a recall- or field-correction situation.

At the summit, you will hear industry case studies and featured topics, including:
• Current state of recalls and assessment of FDA expectations
• Industry approaches and best practices for drug and device recalls
• Global regulatory landscape and the impact of varying international expectations
• Communication strategies for effectively disseminating recall information
• How to train cross-functional business teams on effective execution of product recalls

Distinguished speakers include Cecilia Wolyniak, recall team leader at the Office of Enforcement, Division of Compliance Management and Operations, at the Food & Drug Administration (FDA); and James Tillman, RAC, vice president of Quality and Regulatory Compliance Initiatives at Danaher Corp.

Learn more and register here.

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About The Author

CBI

CBI, an Advanstar company, is the leading provider of market-driven, unbiased conferences for the pharmaceutical, biotechnology, medical device, and health care industries. CBI offers specialized information presented in interactive formats by thought leaders and regulators. Visit online at www.cbinet.com

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