How to be Well Prepared to Host a Regulatory Audit

The term “audits” and what it implies, whether performed by regulatory auditors, internal audit teams or third party customers, often invokes both anxiety and questions as to how best to prepare for them. The more a company prepares for an audit, the more likely the results will be to their benefit.

Getting through a regulatory audit and how to prepare for it, is vital for companies to know and often helps determine the direction of the audit. Preparation is key as well as knowing what inspectors will focus on and actions to avoid. This webinar will give attendees a template to use to help devise a training program to those responsible for meeting inspectors, the audit team, those who will deal with inspectors as well as upper management. Finally, after getting through an audit, observations made still need to be responded to and this webinar will give suggestions as to how best to address them.

This webinar will help establish an outline for both the preparation for an audit, along with recommended practices for hosting one. Topics covered will include items to address prior to the audit, during the audit and actions required once the audit has been completed. Attendees will be given the chance to ask questions relating to past experiences with auditors along with questions they may have in anticipation of an upcoming audit. Common audit techniques used by auditors to gather information will be reviewed along with practices to avoid during an audit.

Areas Covered in the Session :

  • Review the items that need to be in place prior to an audit
  • What to expect during the opening meeting and how to control the audit to your advantage
  • Practices to implement during the audit and those that need to be avoided
  • Learn typical audit techniques by investigators and how best to handle them
  • Learn what your responses should include prior to submitting to the agency for review
  • Interactive Q&A Session
Who Will Benefit:

  • QA/QC Departments
  • Manufacturing Departments
  • Engineering Departments
  • Validation Departments
  • Regulatory Departments
  • Management Teams

FDB1965

Kenneth Christie

Kenneth Christie has over 30 years of sterile manufacturing and regulatory GMP consulting experience in the areas of Quality Assurance and Validation Management in the pharmaceutical and biotechnology industries. Mr. Christie is currently the Chief Operating Officer for VTS Consultants, Inc. located in Amherst, MA. Specifically, his responsibilities include quality system auditing, GMP training, and serving as a subject matter expert for aseptic manufacturing processes, medical devices, APIs and solid dosage processing equipment, utilities, and systems on a global basis. Mr. Christie also performs vendor audits, site pre-approval inspections and assists clients with addressing and correcting regulatory observations.

Mr. Christie was the Validation Manager at Parke-Davis’ Sterile Products Facility where he was involved in the review and approval of all facilities, equipment, and system commissioning/qualification activities. He had routine interaction with the FDA and European inspectors (EMEA), corporate management and third party contract-manufacturing representatives to defend validation practices and to assure regulatory compliance for the manufacture of aseptically produced products.

Mr. Christie is a speaker and trainer for several professional organizations in the US, Canada, Europe, and Asia and is a published author of several articles dealing with the challenges of aseptic processing. Additionally, Mr. Christie served as a member of the ISPE’s Professional Certification (PCC) Commission as an Examination Development Committee (EDC) member.

He possesses a BS degree in Biology from Shippensburg State University (PA) and an Executive MBA degree from Michigan State.

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  • Login Information with Password to join the session, 24 hours prior to the webinar
  • Presentation Handout in .pdf format
  • Presentation from the Speaker
  • Feedback form
  • Certificate of Attendance
  • Recording access Information with Password to view the webinar, will be sent 24 hours after the completion of the Live webinar.
  • Presentation Handout in .pdf format
  • Certificate of Attendance