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Medical devices, especially implantable and long-term wearables, demand extreme reliability, ultra-low power consumption, and robust fail-safe mechanisms. Achieving sub-10µA power operation, hermetic sealing, and high-reliability components is crucial for ensuring longevity, biocompatibility, and regulatory compliance.

Health Level 7 (HL7) is a set of standards that enable the exchange of healthcare data between different systems. Over the years, HL7 has evolved from version 2 (HL7 v2) to version 3 (HL7 v3), with each iteration aiming to improve interoperability and data standardization. However, the adoption of these versions has varied significantly across the industry.

Wearable medical devices are revolutionizing remote patient monitoring, disease management, and clinical trials. However, their success depends heavily on firmware development the embedded software that controls sensors, manages power, and ensures seamless connectivity. Designing robust firmware for these devices requires balancing low power consumption, real-time data processing, security, and regulatory compliance.

From prototype to product: scale smart, stay compliant, know your buyer, and build on a strong clinical foundation.

As CI/CD pipelines grow more critical to engineering velocity, staying informed in real-time becomes essential. At ITR VN, we rely on seamless notifications between Jenkins and Microsoft Teams to track deployments and resolve issues quickly. With Microsoft phasing out the Office 365 Connector, many teams face disruption. Here's how we transitioned smoothly using Power Automate—without changing a single Jenkins job.

Discover why early-stage MedTech startups regret not integrating ISO 13485 before MVP development. Learn how this quality standard ensures compliance, reduces costs, and accelerates market entry for medical devices.

Learn about FDA Class 3 medical devices, their high-risk nature, regulatory requirements, and compliance strategies. ITR VN supports manufacturers in navigating the complex Premarket Approval (PMA) process for market success.

Discover FDA Class 2 medical devices, their regulations, real-world examples, and effective compliance strategies. ITR VN supports FDA-compliant device development, ensuring safety and market readiness.

On April 15, 2025, representatives from ITR held an official meeting with the Institute of Biomedical Physics, an entity under the Military Medical Department of the General Department of Logistics, at the Institute’s headquarters. The meeting served not only as a platform for both sides to share their capabilities but also to lay the groundwork for a strategic collaboration in the development of EMG (Electromyography)-based medical devices - a technology with immense potential in rehabilitation and personalized healthcare.