At Suntra MedTech Solutions, we believe innovation doesn’t stop at the lab bench. Our Knowledge Center is where engineering insight meets industry perspective. It is a hub for medtech leaders looking to stay ahead of what’s next.
Explore our expert-driven content including blogs, articles, solution sheets and white papers. These are all designed to share what we’ve learned, spark new thinking, and help you navigate the complex path from concept to care.
How workflow, IT integration, and reimbursement gaps stall promising devices—and what to do about it In 2011, when the early AI engine IBM Watson won a three-game exhibition tournament of Jeopardy, besting two human contestants who were widely considered to be the greatest ever to play the game, it was considered a real breakthrough for […]
Healthcare collects more data than any industry on earth. Most of it never gets used. Here’s why that paradox persists, and what has to change. Healthcare data is growing at 36% annually, faster than financial services, faster than media. Yet the majority of what gets collected sits idle, generating cost and complexity without generating insight. […]
The Hippocratic Oath and its famous dictum, “First, do no harm” (primum non nocere), have been part of the medical world for centuries, a telling sign of medicine’s long-standing commitment to prioritizing the welfare of the patient. But what it meant to “first, do no harm” back in the day when care was dictated almost […]
New product development processes that are overly siloed are stifling medtech innovation. Here’s why and the steps you can take to get engineering, clinical, regulatory, marketing, and manufacturing all working in parallel from day one.
In emergency medicine, minutes matter. But behind every “rapid response” clinical innovation is years of disciplined systems thinking, engineering rigor, and regulatory foresight. One of the most complex challenges facing trauma care today isn’t treatment, it’s access. Plasma, a critical component in emergency transfusions, has traditionally been constrained by freezing, storage, transport logistics, and slow […]
There’s no longer a debate about AI having an impact on healthcare. While we’re still in the early stages of the AI revolution, it’s now the rare clinician or patient who has not encountered an FDA-approved AI solution for some aspect of medical care, such as interpreting MRI images or analyzing electro-cardiograms. The problem is […]
New product development processes that are overly siloed are stifling medtech innovation. Here’s why and the steps you can take to get engineering, clinical, regulatory, marketing, and manufacturing all working in parallel from day one.
On November 6, Suntra MedTech Solutions President Bryan Gilpin joined Paul LaViolette, Managing Partner at SV Health Investors and former COO of Boston Scientific, for a fireside chat hosted by MassMEDIC. The discussion brought together decades of experience, sharp insights, and a shared commitment to shaping the next era of medtech innovation.
New product development processes that are overly siloed are stifling medtech innovation. Here’s why and the steps you can take to get engineering, clinical, regulatory, marketing, and manufacturing all working in parallel from day one.
Bringing a new product to market is an exciting journey—but one filled with risks that can derail even the best-laid plans. In our latest blog, Navigating the Product Development Maze: The Essential Role of Risk Management, we explore how proactive risk management helps teams stay focused, informed, and aligned at every stage of development. Learn how setting clear goals, evaluating multiple concepts, and building a flexible project plan can drive your product’s success. For an in-depth guide to mastering each phase, download our whitepaper, New Product Development: Managing the Risks.
The landscape of medical device cybersecurity has officially changed. The transition from a framework based on “shoulds” to one defined by “musts” has raised the bar for regulatory compliance, security rigor, and patient safety. The FDA’s updated guidance on cybersecurity in medical devices. At Sunrise Labs, we are proud to announce that our Secure Product […]
In the rapidly evolving landscape of medical device development, risk management is a fundamental process that ensures patient safety and regulatory compliance. An effective risk management strategy not only identifies potential hazards early but also streamlines development by reducing costly redesigns and regulatory hurdles. Understanding Risk Management Risk management, as defined by ISO 14971, is […]
