Aspects to Consider For Clean Room Qualification And Operation – Webinar By Globalcompliancepanel
Overview: Controlled environmental conditions are often used when making medical devices and pharmaceuticals. However, to make sure these clean rooms are continuously operating in a state of control can be a difficult task unless the appropriate controls are incorporated into the design.
This talk will focus on the controls that need to be considered during the design and contruction and the methods to demonstrate these controls are effective.
Areas Covered in the Session:Clean Room Classification Design and OperationEngineering and Budget ConsiderationsAir Filtration and Maintaining Positive PressureInterlocks and Pass ThroughsControlling Human FactorsAcceptance CriteriaWho Will Benefit: This discussion will benefit any organization that wants to improve the control of their current clean room faclity or those considering building or upgradeing their clean rooms. It should be of interest to:QA and Manufacturing ManagersEngineersSupervisorsconsultantsAuditors
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
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Tuesday, May 15, 201210:00 AM PDT | 01:00 PM EDT
Price List:Live : $245.00Corporate live : $995.00Recorded : $295.00
Phone: 800-447-9407Fax: 302-288-6884