Freyr Solutions Launches State-of-the-Art Human Factors Engineering Services

New Jersey – 13-09-2024  – Freyr Solutions is excited to announce the launch of its Human Factors Engineering (HFE) services, a game-changer in the medical device industry. With this new offering, Freyr Solutions is committed to helping medical device manufacturers create products that are not only compliant but also intuitive and safe for users.

Our HFE services are designed to address one of the most pressing needs: use-centric designs. We focus on understanding user behaviours, conducting rigorous usability testing, and refining designs to meet the highest regulatory standards, including FDA and ISO. This isn’t just about compliance; it’s about ensuring that medical devices truly meet the needs of the people who use them.

"At Freyr, we believe that innovation and user safety go hand in glove. Our new Human Factors Engineering services are a reflection of that belief, in a bid to help clients develop devices that will make a real difference in the lives of people," said Suren Dheenadayalan, CEO of Freyr Solutions.

This new service offering is designed to assist in the development process of manufacturers by monitoring potential user problems early in the development cycle, reducing the risk of expensive redesigns and product recalls. In addition, as regulatory bodies like the FDA begin to focus on usability, Freyr’s HFE services provide clients with a competitive edge in the market.

By integrating human factors engineering into the product lifecycle from the very beginning, Freyr Solutions not only ensures compliance but also optimizes the overall user experience, leading to safer, more effective medical devices. This holistic approach is expected to foster greater trust and satisfaction among end-users, ultimately driving better health outcomes.

About Freyr

Freyr Solutions is the largest global Regulatory solutions and services company that offers end-to-end Regulatory solutions to life sciences industries. The services include Regulatory affairs, pharmacovigilance, clinical research, quality management, and technology solutions such as Regulatory information management systems and Regulatory data integration. Freyr's expertise in Regulatory affairs makes it a trusted partner for life sciences companies seeking to navigate the complex Regulatory landscape.

  • 14+ years in the life sciences Regulatory landscape.
  • 1600+ global customers and growing.
  • 2100+ in-house Regulatory experts.
  • Global presence across 20+ countries.
  • 850+ in-country Regulatory affiliates across 120+ countries.
  • ISO 9001 & ISO 27001 Certified.
  • ISO 27001 Certified for information security management, state-of-the-art infrastructure.