Forum - Miami, Florida
With increasing scrutiny and inspections from the FDA, manufacturers continue to face challenges surrounding potential audits, audit corrections, and internal procedures developed to sustain a robust and compliant manufacturing facility.Learning from leaders in quality assurance and regulatory affairs with dozens of years of experience will be of great value to attendees, as presenters share their expertise and insight into the development and maintenance of highly compliant facilities. Sessions will cover topics related to preparations for audits, strategies for maintaining composure during audits, as well as internal programs that can be developed and conducted in order to maintain regulatory readiness.
Sunday, January 22, 2012 to Tuesday, January 24, 2012
Miami, Florida, U.S.A.
Contact: (phernandez@q1productions.com)
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