Webinar on Writing Effective SOPs for Medical Device Quality Management Systems
Website https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=MD1637 |
Category Medical Devices
Deadline: July 22, 2106 | Date: July 22, 2106
Venue/Country: Online, Canada
Updated: 2016-06-30 18:43:05 (GMT+9)
Call For Papers - CFPThis webinar will help you to write clear, unambiguous, yet 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 Session :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 SpecialistsSubject Matter Experts and others writing proceduresInternal 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 requirementsDirectors, VPs, and others attending management review
Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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