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FDA Audit Preparedness
Date: June 12, 2009
Location: Los Angeles
SoCalBio Regulatory Best Practice Workshop. California inspections from device, pharma and IVD experts. This full day training session will cover 483 responses, warning letter responses and Consent Decrees and how to avoid them. Additionally we will cover best practices in hosting regulatory inspections and best practices for self inspection. See https://s08.123signup.com/servlet/SignUp?PG=1522578182400&P=1522578133581343158716400&Info=
More information: https://s08.123signup.com/servlet/SignUp?PG=1522578182400&P=1522578133581343158716400&Info=
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