Tuesday, October 29, 2019

Graphic about the AMD Summit in ChicagoAmerican Medical Device Summit 2019
Hyatt Regency O’Hare
Chicago, IL
October 28–29, 2019

Bill Stamm, VP of General Digital Software Services, will be exhibiting and conducting a workshop at the 2019 American Medical Device Summit. He looks forward to engaging with attendees and representatives from medical device companies, and discussing how our product development, with a focus on the full Software Development Life Cycle, can help them meet their needs within budget.

The workshop takes place on Day 1 at 3:00 PM and the topic is: 
Software Enhancements: Distinguishing Type & Development to Meet Requirements of Safety, Functionality and Cybersecurity
  • Why software has become an important part of all products, integrated widely into digital platforms that serve both medical and non-medical purposes
  • Differentiating between the two types of software related to medical devices include software that is integral to a medical device (Software in a Medical Device) and software used in the manufacturing
  • Providing a strategy to develop SaMD and software as part of medical device or combination product systems
Watch videos of our workshop from 2018!

About General Digital Software Services
GDSS is a company that, for over 45 years, has been dedicated to product development with a focus on the full Software Development Life Cycle, including: software development, certification and testing [Independent Validation and Verification (IV&V)] — in the most stringent safety critical environments in the world: medical [FDA, IEC62304, PMAs, and 510(k)], industrial controls [IEC 61508, IEC 61131], aerospace and avionics [DO178], pharmaceutical and general packaging, and robotic equipment.

About the Summit
Setting the standard on how the industry should connect and exchange ideas, the American Medical Device Summit provides insights and strategies to enhance the professional development of executives involved in the design, product development, innovation, technology and quality/ regulatory aspects of medical devices.


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