Forbes contributors publish independent expert analyses and insights. I write about finance and technology. This article is more than 5 years old. As financial services grow more complex — think ...

As semiconductor devices become smaller and more complex, the product development lifecycle grows increasingly intricate. So, from early builds to pre-qualification testing, firmware development and ...

In an age where software drives nearly every aspect of daily life, ensuring its quality at scale has never been more essential. In 2024 alone, global IT spent over $5.1 trillion in expenditures, and ...

InstantGMP™, a provider of cloud-based GMP and FDA compliance software for pharmaceutical and other regulated manufacturers, announced it has aligned its software development and validation practices ...

The FDA recalled 60 medical devices last year, and the running total for this year is 56. The good news is that there’s a startup working to make future totals lower. The startup, named Ketryx, ...

Risk is a lens, not a leash. Once teams see what truly threatens patients and processes, the busywork falls away, and quality ...

The advent of artificial intelligence (AI) and data-driven methodologies has triggered a wave of transformation in regulatory compliance and quality assurance for the development of medical devices.

When it comes to software development projects, business leaders and consumers alike tend to believe the sooner it’s done, the better. While speed is imperative, demanding an abbreviated turnaround ...

In my role at Inspired Testing, I speak with clients across multiple industries every week. From financial services to retail, healthcare to logistics, there's one issue that surfaces in nearly every ...