5th Human Factors Engineering and Usability Studies Summit 2020

Topics

• Risk management methodologies for anticipating product errors
• Strategies for recruiting ideal user groups while meeting budgets and deadlines
• Surefire skills for creating and submitting the templates necessary to document regulatory compliance
• Techniques to improve the validation testing and user interface of medical device software
• Key elements for ensuring devices have been validated for users with special needs

Who should Attend

Medical device, biotech, and pharma professionals with responsibilities in:

• Usability / User Experience / User Interface / UX / UI
• Human Factors / Human Factors Engineer
• Medical Device / Device Design / Device Development / Device Technology
• Combination Products / Combo Products
• Product Development
• Design Assurance Engineer
• Wearable
• Handheld
• Technology / CTO
• Pharmaceutical Development Operations
• Customer Experience
• R&D
• Design Controls
• Engineering / Device Engineering / Clinical Engineering
• Validation
• Industrial Design
• Instrumentation
• Packaging / Labeling
• Regulatory Affairs / Regulatory CMC
• Quality / Quality Control / Quality Assurance / Quality Engineer
• Pharmacovigilance
• Risk Management
• Marketing / Brand Management
• Software Engineering / Software Management / Software Development
• Pharmaceutics
• Clinical Affairs / Clinical Research / Clinical Development
• Brand Manager

Also:

• Medical Device / Combination Product Design & Engineering Specialists
• Human Factors Specialists
• CROs / Regulatory Specialists