FDA Compliance 2012 - Prepare for Tougher U.S. FDA cGMP Compliance Audits
Date2012-02-07
Deadline2012-02-07
VenuePalo Alto, USA - United States
KeywordsFDA cGMP guidelines; FDA cGMP compliance audits; FDA cGMP audit; FDA audit training; FDA audit preparation; good manufacturing practices compliance
Topics/Call fo Papers
This FDA cGMP training webinar will discuss US FDA’s approach to cGMP Audits and expectations from companies. It will also evaluate chief concern areas of cGMP compliance audit and anticipatory emphasis changes as per new regulatory climate.
Why Should You Attend:
Recent audits indicate the past ways of doing things will no longer be acceptable. Increasingly reports from the field indicate that the Agency is using high-profile cases to drive compliance to smaller companies and suppliers. Recent events in regulated industries indicate a public's growing dissatisfaction with what they view as a lack of oversight of business by regulatory agencies, including the FDA.
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Last modified: 2011-12-26 17:19:39