How FDA Trains Its Investigators to Review CAPA, and What You Can do to Prepare 2017

How FDA Trains Its Investigators to Review CAPA, and What You Can do to Prepare 2017 is a webinar that covers topics such as:

• CAPA Implications of Investigations Operations Manual (IOM), and Recommended Methods of Compliance for each Requirement
• Documents Used by FDA Inspectors
• QSIT Manual: Description of each CAPA Inspectional Objective, and Recommended Methods of Compliance
• CAPA Implications of CPG Manual 7382.845, and Recommended Methods of Compliance for each Requirement

How FDA Trains Its Investigators to Review CAPA, and What You Can do to Prepare 2017 brings together attendees from Diagnostic, Medical Device, Biologics and Pharmaceutical fields, including Regulatory Management, Executive/Senior Management, Any personnel who may have direct interaction with FDA officials, QA Management, Quality System Auditors and Consultants.