by Waltteri Sorvisto | May 7, 2026 | Medical Device Services
Medical device development often begins with a strong technical idea. For startups, that early momentum is important. A prototype, a clinical need, or a promising technology can create the energy needed to move a product forward. But in medical device development,...
by Waltteri Sorvisto | Apr 29, 2026 | Product & Compliance
Medical device software is often discussed primarily as a development challenge. The focus tends to be on functionality, performance, architecture, and how the final product will behave in use. All of that matters. But in regulated environments, software development...
by Waltteri Sorvisto | Apr 23, 2026 | IPR
In product development, intellectual property is often discussed relatively late. The conversation tends to begin when an invention is ready to be protected, a filing strategy is taking shape, or external investors start asking how the company plans to defend its...
by Waltteri Sorvisto | Apr 16, 2026 | Medical Device Services
For medical device and IVD manufacturers in Europe, EUDAMED is moving from something to prepare for into something that must be actively managed. The timeline is now clear. Following the European Commission’s notice that the first four EUDAMED modules are functional,...
by Waltteri Sorvisto | Apr 9, 2026 | Commerzialisation
The Cyber Resilience Act (CRA) introduces a new layer of requirements for products with digital elements, with the goal of improving cybersecurity across the EU market. For many companies, the structure of CRA will feel familiar. It places responsibility on...
