RAPS Approved Webinar
Sterilization as a Benchmark for Cleaning Validation and Control
Date & Time: Course "Sterilization as a Benchmark for Cleaning Validation and Control" has been pre-approved by RAPS as eligible for up to 1.00 credits towards a participant's RAC recertification upon full completion.
Instructor Profile: Wednesday, September 26, 2012
10:00 AM PDT | 01:00 PM EDT
Duration: 60 Minutes
Instructor: Anthony DeMarinis
Price : $245.00
(for one participant)
Overview: Cleaning validation is increasingly important in preventing cross contamination and interactions between active ingredients in subsequent batches run in the same equipment. This webinar will review principles of sterilization validation and using them as a benchmark for more robust cleaning validation. Emphasis will also be placed on interrelationships with other processes and using the information gained during validation to monitor and control the cleaning process to prevent failure.
Areas Covered in the Session: l
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Sterilization process description and validation options including the kinetics of lethality (bioindicator vs bioburden) and test methods Pre-validation activities including defining worst case challenge to the process and selecting cleaning agents. Aspects to consider when writing the validation protocol. Sources of process variation and basics of process control Data collection and troubleshooting Post-validation (re-validation) and change control Reporting and documentation requirements
Anthony DeMarinis Quality Systems Manager, Sealed Air Tony has BS degrees in Biology & Microbiology and a MS in Quality Management. He is currently Quality Manager at Sealed Air, a supplier of rigid medical device packaging solutions. Previously he was Quality Systems Manager at Davol, Director of Quality Assurance at Scott Laboratories and Sr. Microbiologist at the National Cancer Institute. He is a Certified Quality Auditor-BioMedical and Certified Manager of Quality and Organizational Excellence by the American Society for Quality. He also teaches the refresher courses for these certification programs through the local RI-ASQ section. Tony has over 20 years experience using quality management techniques and value added auditing including the use of Failure Investigation and Root Cause Analysis to improve processes and products...more
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Click here to register for this webinar Who Will Benefit: This webinar will benefit any organization that wants to validate and improve the effectiveness of their cleaning processes. Those who will benefit include QA and Manufacturing Managers and Engineers
who are responsible for validating cleaning or sterilization processes, Consultants, Auditors and responsible executives. It would be really nice if you can circulate this mail to all your deserving colleagues who can immensely benefit from this program. For more information, please contact the event coordinator. We look forward to seeing you at the webinar. Best regards, Event-coordinator GlobalCompliancePanel
About GlobalCompliancePanel GlobalCompliancePanel is an online knowledge fulfillment community portal & it has put together a new model for online compliance training by creating a single window of learning opportunities for compliance professionals & providing a forum for expert speakers/panelists to render their services through simplified online training delivery mechanisms. Our commitment is give compliance regulatory training, showcasing of best industry practices & quality enrichment training sessions in a most cost effective manner. Compliance professionals can benefit from a wide range of training sessions, giving a diverse choice of events & all sessions being either Live or recorded stream or in the form of audio CDs. GlobalCompliancePanel portal ensures a secure & cost effective online environment and also support your E-learning and development on/through our website. Keep track of all webinars arranged for your industry through notifications & event calendars being mailed to your inbox. GlobalCompliancePanel opens new doors of learning opportunities for professionals. GlobalCompliancePanel www.globalcompliancepanel.com
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Published on Sep 13, 2012
Published on Sep 13, 2012
Cleaning validation is increasingly important in preventing cross contamination and interactions between active ingredients in subsequent ba...