NSF International dietary supplement expert Ed Wyszumiala will present at Vitafoods Europe this week on good manufacturing practice (GMP) considerations specific to European dietary supplement manufacturers.
“Good Manufacturing Practice (GMP) in the USA – FDA's Role and Compliance Update”
Presented by: Ed Wyszumiala, General Manager, Dietary Supplement Certification Programs, NSF International
Thursday, 24th May 2012, 12.50h – 13.20h at the Vitafoods Supplier Seminar Theatre
Ed Wyszumiala has more than 10 years of experience in the dietary supplement industry with expertise in product certification and international dietary supplement regulations. As a leading authority on GMP compliance, Ed’s presentation will provide companies with key insights into achieving GMP compliance, which is crucial for European companies that sell products in the U.S. market.
His presentation will also recap the top GMP nonconformances found by U.S. Food and Drug Administration (FDA) inspectors. This information is essential, as the FDA has observed GMP deficiencies in nearly one out of four facilities they have audited in the last two years, providing attendees an opportunity to learn and avoid the costly mistakes made by other companies.