(FDAnews: Falls Church, VA) -- The interactive workshop, Clinical Quality Assurance Roles and Responsibilities for Auditors and Managers, scheduled for Nov. 7–8, 2011, at the Radisson Hotel in Boston, is presented by MSceppa Consulting, provider of quality assurance consulting and auditing for pharmaceutical and biotechnology industries, and FDAnews, provider of domestic and international regulatory, legislative, and business news and information for industries regulated by the U.S. Food and Drug Administration (FDA).

Now you can learn how to FDA-proof your clinical quality assurance (CQA) audits, eliminate costly mistakes, and avoid FDA warning letters that say,“You failed to obtain and document that valid informed consent was obtained for each of the subjects enrolled in the study as required by stated regulations.”

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