Listings tagged with 'FDA warning letters' (9)
Overview: When validated methods are transferred between laboratories and sites, their validated state should be maintained to ensure the same reliable resul...
Description : The success of an audit by federal regulators does not always depend on the level of training provided to staff and department employees, but al...
Speaker: John E. Lincoln Key Take Away: Learn how to minimize the chance of receiving an FDA Warning Letter, what to doing during and after an FDA complia...
Description : This live training webinar will discuss the just issued (July 2015) DRAFT Guidance for Industry on “Request for Quality Metrics” along with how ...
Description : To achieve and remain compliant with the adequate use of the Excel spreadsheet in FDA-regulated environments, it is critical that laboratory per...
Description : This 90 minute in-depth webinar discusses the FDA Warning Letters and recent high-profile recalls indicate major cGMP deficiencies in big name d...
Overview: FDA investigations can lead to observations requiring remediation, disruption of your business, loss of revenue and enforcement actions up to and i...
Overview: There is an on-going major shift in the emphasis of Federal Drug Administration cGMP audits. These changes in focus have a major impact on indiv...
Note: This Webinar covers topics relevant to both drugs AND devices. FDA is more vigilant and aggressive than ever before with its 483 and warning letter enf...
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