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Second ISPE-FDA Event Attracts Top Names, Features Release of Drug Shortage Survey Results
Date:4/16/2013

TAMPA, Fla., April 16, 2013 /PRNewswire/ -- ISPE announced today that it will hold its second annual Redefining the "C" in CGMP conference, 11 – 13 June in Baltimore, Maryland USA. Themed "Ensuring a Reliable Supply of Quality Medicines," the event will feature strategic education on issues of interest to industry leaders and global regulatory officials focused on quality systems, processes and technology utilization that drive quality enhancements that support a reliable drug supply.

"This event is where industry and regulators must come together to share their views on contemporary regulatory issues and solutions," said ISPE President and CEO Nancy Berg . "The sessions, case studies and workshops will be focused on how great companies are establishing and sustaining a culture of quality through contemporary quality management strategies, new methods and technologies, metrics and more effective approaches to integrating suppliers into quality systems."

The event will feature top speakers from the pharmaceutical industry and regulatory agencies, including:

  • Howard Sklamberg , Director, Office of Compliance, US FDA
  • Andy Skibo , Regional Vice President, Biologics-Supply, MedImmune/AstraZeneca
  • Gerald Heddell , Director of Inspection, Enforcement and Standards, MHRA, UK
  • John Pinion , Senior Vice President, Quality/Compliance, Genentech, Inc.
  • Zena Kaufman , Senior Vice President, Global Quality, Hospira
  • Cindy Salamon , Vice President, Global Quality Services, Bristol-Myers Squibb
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SOURCE ISPE
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