Current Good Manufacturing Practices (cGMPs) in a regulated industry require the use of controlled documents. Participants in this course will learn strategies for designing and writing controlled documents, with the goal of minimizing risks for misinterpretation, and errors in communication. Participants will also gain an understanding of the associated regulatory requirements, and will learn fundamental concepts of document control.
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9/30/2016
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When:
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09/30/2016 10:00 AM - 12:00 PM
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Where:
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Biotility at UF’s Center of Excellence for Regenerative Health Biotechnology 13706 Innovation Drive Alachua, Florida 32615 United States
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Contact:
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Tamara Mandell
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« Go to Upcoming Event List
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Please visit http://biotility.research.ufl.edu/biotility-calendar for more information.
Please register here https://xms.dce.ufl.edu/reg/groups/CERHB/default.aspx?program=259&filter=&filtervalue=.
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