Conference Details

The growth of the medical software industry outpaces the design of FDA's regulatory process. In some instances clinicians have weighed the risk of software failure against the benefits of using a device at all. Device software is often used in conjunction with other software-based devices, but their interoperability was never anticipated.

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Place : United States, San diego

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Contact Person:Paula Edwards

Description:

The growth of the medical software industry outpaces the design of FDA's regulatory process. In some instances clinicians have weighed the risk of software failure against the benefits of using a device at all. Device software is often used in conjunction with other software-based devices, but their interoperability was never anticipated.

The growth of the medical software industry outpaces the design of FDA's regulatory process. In some instances clinicians have weighed the risk of software failure against the benefits of using a device at all. Device software is often used in conjunction with other software-based devices, but their interoperability was never anticipated. will be held in San diego,United States on date 2017-11-17

Deadline for abstracts/proposals : 15th November 2017

Organized By :New York Events List

Keynote Speakers : Former Associate Center Director of FDA's CDRH Casper (Cap) Uldriks, through his firm “Encore Insight LLC,” brings over 32 years of experience from the FDA. He specialized in the FDA’s medical device program as a field investigator, served as a senior manager in the Office of Compliance and an Associate Center Director for the Center for Devices and Radiological Health.

Conference Highlights :Understanding FDA legal authority Applying FDA classifications / risk controls Understanding FDA and NIST software guidance Identifying the quality system regulation for risk management, software verification and validation Identifying cybersecurity issues and developing a planned response Identifying and resolving interoperability issues

Venue :San Diego, CA, United States

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The growth of the medical software industry outpaces the design of FDA's regulatory process. In some instances clinicians have weighed the risk of software failure against the benefits of using a device at all. Device software is often used in conjunction with other software-based devices, but their interoperability was never anticipated.

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