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Quality Audits in the (Bio)Pharmaceutical and Device Industry | Alachua
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When: 09/18/2017
1:00 PM - 3:00 PM
Where: Biotility at UF CERHB
13706 Innovation Drive
Biotility Education Center: Lab 403
Alachua, Florida  32615
United States
Contact: Tamara Mandell

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Quality Audits in the (Bio)Pharmaceutical and Device Industry

External and Internal Quality Audits in GMP manufacturing including the (bio)pharmaceutical and medical device industries are global regulatory compliance tools to ensure the safety and effectiveness of drugs, vaccines, other biological products, and devices. The course includes an overview of regulatory requirements, the different types of audits, and how to prepare for, conduct, and follow up on an audit. Special attention will be given to the internal audit which is a company's most important managerial tool for monitoring the quality of processes and products. Internal audits, when effectively implemented, are critical to the identification of weaknesses and the continual improvement of the Quality System.

DATE: Monday, September 18, 2017                 TIME: 1:00 p.m. 3:00 p.m.         REGISTRATION FEE:  $95                                Register Now

About BioFlorida

BioFlorida represents nearly 6,000 establishments and research organizations in the biopharmaceutical, medical technology and bioagriculture sectors that collectively employ nearly 83,000 Floridians.


Members of the BioFlorida network include emerging and established life science companies, universities, research institutions, hospitals, medical centers, incubators, economic development agencies, investors and service providers.


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