#change computer systems

Summary:GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize a RAPS pre-approved webinar on the topic, €Configuration Steerage and Change Experimentation for Computer Systems€ on November 14. This 75-minute webinar earns up versus 1.25 RAC credits towards a participant's RAC recertification upon full completion. Dr. Ludwig Huber, Director of Labcompliance and Chief Advisor in order to global FDA compliance at Agilent Technologies, will be the Speaker at this parley. ----------------------------------------------------------------------------------------------------------------- Definition: What happens when changes are made into computer systems? They bring not to mention them problems relating to software, computer systems and networks. It is the same, whether the changes are made during design and cultivation, bar sinister when the systems are being used. Among the most over and over cited deviations during FDA inspections, too many changes of computer systems and failure to adequately chirograph the authorities situation high. There is uncertainty of documentation of procreative set-up and directive changes of yesterday on among the users of systems; view owners and trellis administrators alike. This webinar clears the misunderstanding professionals of computer systems shave of what happens when changes made to the system are not backed in uniformity with adequate rota. Attendees concerning the examination hankering receive glaring recommendations and tools pertaining to how to configure and change computer systems in regulated environments. This trough will offer these guise materials for easy implementation: o SOP: Relief keep of software and calculator systems o SOP: Handling warranty patches o SOP: Change control as for networks - planned and unplanned changes o Six case studies Areas Covered toward the Session: o US FDA and EU requirements for change control o Defining image management vs. change control and change dean o The GAMP IEEE models for configuration management and change control o How headed for keep clear of frequent changes of a digital computer system o Reviewing a change stability strategic plan o Set off control for hardware, operating systems and application software o The trade off control writ for set-up and improvised changes o Dealing with security patches o Versioning respecting software and relay systems o What so test hind changes o How to legal paper changes o Going through examples for hardware, software and networked systems ----------------------------------------------------------------------------------------------------------------- When:November 14, 10:00 AM PDT | 01:00 PM EDT ----------------------------------------------------------------------------------------------------------------- By whom: Ludwig Huber, Ph.D., is Chairman of Labcompliance and Chief Advisor for global FDA compliance at Agilent Technologies. Ludwig is the editor of Labcompliance, the global on-line nest egg for validation and unloathness issues for laboratories. He is the author of many books, including Validation and Tuning in Analytical Laboratories and Validation upon Computerized Analytical and Networked Systems. <\p>

He also has more over against 100 paper publications and conducts online tutorials every hour. His waterworks speak of his erudition and deep understanding of everything that goes into FDA compliance. That Dr. Huber is a superb good judge incidental not unparalleled the FDA nonetheless also irrelative regulatory bodies is evident from the fact that inner self has been The most Advisor on Compendious ISO 17025 and FDA Compliance. <\p>