Webinar Duration: 90 minutes
RECORDED: Access recorded version only for one participant; unlimited viewing for 6 months (Access information will be emailed 24 hours after the completion of payment)
SPEAKER: John (Jerry) Lanese
In this webinar we will discuss CAPA (Corrective Actions and Preventive Actions) , what they are and why the FDA expects the industry to initiate the investigation of any deviation and the complete recommended corrective and preventive actions. We will also discuss the CAPA System, the procedure or family of procedures that manage corrective actions and preventive actions from the observation of a deviation through the verification of the corrective or preventive action.
Why should you Attend: Recent FDA Warning Letters and 483s have included observations the firm’s CAPA program was inadequate. It is important the appropriate staff understand what CAPA is, what constitutes a CAPA program, and what should be included in the program. The objective of this webinar is to inform personnel in the pharmaceutical industry of the growing expectation that each organization have an effective CAPA system that defines process and responsibilities for the identification, recording and investigation of deviations, the recommendation and execution of corrective actions and demonstrating that the action effectively correct and/or prevent the deviation.
Who Will Benefit:
– Laboratory Managers
– Laboratory Supervisors
– Laboratory Analysts
– Quality Assurance Managers
– Quality Assurance Record Reviewers
John (Jerry) Lanese is an independent consultant with a focus on Quality Systems and the components of an effective Quality System. He received a BA and MS from Middlebury College and a Ph.D. in Analytical Chemistry from the University of Michigan and began his career teaching Analytical Chemistry in a small liberal arts college. Dr. Lanese moved from the academic environment to the pharmaceutical industry where he has managed Analytical Research, Quality Control and Quality Assurance functions. In 1994 Dr. Lanese formed his own company, The Lanese Group, and since that time he has been a consultant in the area of quality system and cGMP compliance and has consulted with small and large medical device and pharmaceutical companies, including companies under FDA Consent Decree, API and excipient manufacturers, electronic firms and other manufacturing organizations. Dr. Lanese lectures throughout the world on a variety of topics related to Quality Systems, GMPs, APIs, laboratory operations, calibration, change control, deviations and product reviews for clients and national seminar and conference providers. He was named the Best Seminar Presenter of the year 2001 by the Institute of Validation Technology.
In 2005, his article “Training and the Laboratories” was selected as best article of year by the Journal of GXP Compliance. Recently, in 2007, Jerry received the Kenneth Chapman Industry Recognition Award for his contributions to the Pharmaceutical industry. Jerry is a member of the Editorial Board of the Journal of GXP Compliance. He has been active in the Kansas Award for Excellence program, a Baldrige Criteria based program, for the past fifteen years. He has served as Examiner, Lead Examiner and Judge and is currently the Director of the Kansas Award for Excellence Program. In addition, he served as a Baldrige Examiner in 2008. Dr. Lanese is also a member of American Society for Quality, AOAC and the Institute for Management Consultants and is a Certified Management Consultant (CMC). He is listed in Madison Who’s Who. He was active in the Kansas Award for Excellence program, a Baldrige Criteria based program, for seventeen years. He served as Examiner, Lead Examiner, Judge and the Director of the Kansas Award for Excellence Program. In addition, he served as a Baldrige Examiner in 2008. On the personal side, Jerry is active in two Toastmasters clubs in the Johnson County, KS area, and is the president of Kansas City Ragtime Revelry, an organization that promotes ragtime and early American music.