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Conference Details

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

Date :

Place : United States, Fremont

Website :

Contact Person:Traininng.com LLC

Description:

This webinar will walk you through step-by-step how to complete a DIOM for your product and simplify this often overly complex process, 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 DIOM - A Straightforward Method for Meeting FDA Requirements for Design Inputs and Outputs will be held in Fremont,United States on date 2019-05-31

Deadline for abstracts/proposals : 31st May 2019

Organized By :Traininng.com LLC

Keynote Speakers : 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 compan

Conference Highlights :Introduction to the DIOM template How to identify your design inputs How to categorize your design inputs and their sources Ways in which design inputs can be verified Common documents and activities used as design output evidence Additional requirements of design inputs and outputs

Venue :Fremont, CA, USA

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

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