Secrets to Writing Effective SOPs for Medical Device QMS
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Website http://c2gowebinars.com/product/?topic=sop-qms |
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Category Medical Device
Deadline: February 23, 2016 | Date: February 23, 2016
Venue/Country: Online, U.S.A
Updated: 2016-02-09 19:10:10 (GMT+9)
Call For Papers - CFP
DESCRIPTIONThis webinar will help you ensure that your procedures that are complete, concise, and easy to follow. The FDA expects Medical Device manufacturers to “establish and maintain procedures”. You will learn what this means and how to comply with expectations.Why you should attend:Standard Operating Procedures (SOPs) are a basic ingredient of an effective quality management system. Yet, “inadequate SOP” observations still rank among the most frequently cited 483 and Warning Letter observations. SOPs are one of the first things an auditor/ investigator will review during and inspection. Well written SOPs send a message that your QMS is complete, accurate, and followed.This webinar will help you to write clear, unambiguous, and flexible SOPs. You will learn techniques for creating easy to read, clear, and concise SOPs that your employees can easily follow. Well written SOPs ensure that your employees understand and consistently follow processes. Areas covered in the Webinar:This 90-minute webinar will focus on how to write clear concise SOPs that your employees can follow. Topics to be covered include:FDA and NB expectations for SOPsLessons Learned from 483s and warning letters Common problems with SOPsHow to structure your QMS and SOPsHow to outline and format your SOPsUsing process maps to make procedures clearUsing diagrams and visualsMaintaining and controlling SOPsEnsuring adequate training to your SOPsBest PracticesWho will benefit:Quality Systems SpecialistsDocument Control SpecialistsQuality and Compliance SpecialistsInternal Auditors and ManagersTraining SpecialistsCAPA SpecialistsSupplier Quality Engineers and AuditorsQuality/Compliance managers or directors for Medical Device companiesGeneral Managers wanting to learn how to understand Quality System requirementsWebinar includes:Q/A Session with the Expert to ask your questionA copy of the PowerPoint slides90 Minutes Live PresentationAttendance of Certificate
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