Filter by category:
May 13, 2016
White Paper
Cybersecurity and Design: Managing New Risks and Requirements
Manufacturing has been traditionally perceived as having lower cybersecurity risk than retail or financial businesses with large volumes of consumer information on hand. But the cybersecurity landscape is evolving—hackers are setting their sights on new industries and areas of weakness, while more robust standards and new federal programs are raising awareness among clients and prospective customers.
February 11, 2016
White Paper
Navigating the Medical Regulatory Landscape
In the exclusive Q&A, Navigating the Medical Regulatory Landscape, experts discuss top issues and processes from constant regulatory change to non-compliance risks. Leverage years of industry experience across sectors, and learn a variety of insights and tips to help deepen your knowledge on medical regulations and standards for your next product.
February 2, 2017
White Paper
Legacy Parts: Making the Mission-Critical Decisions
With component life cycles growing increasingly shorter, knowing the right questions to ask can help minimize growing replacement costs. This infographic offers insights to help you overcome component obsolescence and presents key questions you should be asking to resolve product change notifications.
November 29, 2016
White Paper
The Art of Design Verification and Validation: 8 Steps to Creating your Medical Device
Reduce the high cost of medical device development by identifying and fixing critical bugs early in the development lifecycle. This infographic helps you answer the two most important questions: did you design the device right, and did you design the right device? From verifying and validating the design to risk mitigation and software verification, this step-by-step infographic can help you shrink costs while bringing your device to market.
January 5, 2016
White Paper
