Medical Device Software 62304 Compliance 2019

Topics

• Insight into the IEC 62304 standard as it is applied to medical device software
• Providing safe and effective medical devices is in the best interests of all those involved in developing software for these products, and for those involved in developing medical devices that use software
• The current industry best practices that will help you with IEC 62304 compliance
• How to apply this standard to your own work processes

Who should Attend

• IT Developers
• Information Technology (IT) Analysts
• QC/QA Managers and Analysts
• IT Support Staff
• Analytical Chemists
• Clinical Data Managers and Scientists
• Compliance Managers and Auditors
• Quality Managers, Chemists, and Microbiologists
• Automation Analysts
• Lab Managers and Analysts
• GMP Training Specialists
• Computer System Validation Specialists
• Regulatory Affairs Personnel
• Business Stakeholders using Computer Systems regulated by FDA
• Interns working at the companies listed above
• Consultants in the Life Sciences and Tobacco Industries
• This webinar will also benefit any consultants working in the life sciences industry who are involved in computer system implementation, validation and compliance