The DIOM – A Straightforward Method for Meeting FDA Requirements for Design Inputs and Outputs

  • Product Id : MD2990
  • Category : , ,
  • Presenter :
  • Scheduled On : March 20 2019 1:00 pm
  • Duration : 90 Minutes

This webinar will provide valuable insight to design assurance and quality assurance engineers looking to simplify or condense design development activities into one document for easier traceability. This webinar is also ideal for startup companies who are unfamiliar with FDA design development regulations and are looking for a place to start in their path towards compliance.

A robust DIOM can serve as the foundation for meeting FDA requirements and is a useful tool to ensure future iterations, changes, and re-visits to the initial design are clearly documented. A DIOM ensures design information is clearly presented, well-documented, and most importantly, located within one simple document. This webinar provides a simplistic tool to help identify and categorize design inputs, determine the most effective method in providing design output evidence, and showing traceability to all activities associated with both.

The speaker has worked on numerous design development projects in Class II and Class III medical devices as well as establishing Quality Management Systems which include easy-to-understand methods to meet design development and design control requirements. This webinar will walk you through step-by-step how to complete a DIOM for your product and simplify this often overly complex process.

Areas Covered in the Session :

  • Introduction to the DIOM template
  • Better understanding of FDA regulations with regards to design input and output
  • How to identify your design inputs
  • An organized approach in meeting design input and output requirements
  • How to categorize your design inputs and their sources
  • Ways in which design inputs can be verified
  • A simplified way to ensure design inputs and outputs are continually maintained and tracked
  • Common documents and activities used as design output evidence
  • Additional requirements of design inputs and outputs
Who Should Attend:

  • Quality Assurance Departments
  • Quality Control Departments
  • Research and Development Departments
  • Regulatory Affairs Departments
  • Manufacturing Departments
  • Engineering Departments
  • Operations Departments
  • Production Departments
  • Software Developers and Managers
  • Internal Auditors
  • Design Engineers
  • IT Managers and System Administrators
  • Software Quality Personnel
  • Software Test Personnel
  • Software Validation Engineers

MD2990

Denise Wrestler

Denise Wrestler, ASQ CQE, CQA; QA/RA Consultant at CYA Medical Device Consulting, LLC with almost 15 years of experience within FDA-regulated industries including medical device and pharmaceuticals, Ms. Wrestler provides quality, regulatory, and technical expertise to meet individual client needs. Ms. Wrestler agrees with the FDA’s “least burdensome approach” and prides herself on providing options and recommendations for ensuring regulations are met without wasting precious company resources.

Denise Wrestler holds a B.S. in Chemical Engineering with a Minor in Biomedical Engineering from the University of California, Irvine. Additionally, Ms. Wrestler holds ASQ Certifications as a Certified Quality Engineering (CQE) and Certified Quality Auditor (CQA). A contributing author to ASQ’s monthly publication Quality Progress magazine, Ms. Wrestler remains active within the quality and regulatory professional circles to ensure continuing education and awareness within the community. Ms. Wrestler has provided training, workshops, and presentations to small and large audiences alike on topics ranging from QSR, ISO 13485, auditing, and design control to risk management and regulatory readiness and preparation.

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  • Presentation Handout in .pdf format
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