Human-Centered Engineering for Exceptional User Experiences
At Goddard Technologies, we understand that designing medical devices isn’t just about engineering—it’s about creating solutions that transform lives. Our relentless commitment to human-centered design sets us apart in the world of medical technology (MedTech) engineering and design. We put people at the heart of product development, ensuring that every decision reflects the needs, preferences, safety, and experiences of end users while ensuring an accelerated time-to-market for our clients through enhanced validation testing that creates solutions and skirts avoidable product errors from the onset.
Connect with our Experts
In the dynamic landscape of medical device development, user-centric design is paramount. Medical devices require adhering to stringent regulations and standards and an error-proof user experience (UX) and user interface (UI) design. Our approach meets designers and engineers at any step of the development process and places the patient, the healthcare provider, and all stakeholders at the core of every decision. By integrating the voice of every person in your product ecosystem, we ensure that your MedTech solutions don’t just meet regulatory standards but exceed user expectations.
The Result?
Exceptional user experiences that drive unparalleled customer satisfaction, boost market acceptance, and, most importantly, improve patient outcomes.
Goddard’s Medical Device Development Expertise
A successful development journey begins with understanding the intricate interplay between design and user experience. At Goddard, we’ve made it our mission to master these dynamics, providing you with a wealth of knowledge and human factors engineering (HFE) experience, including:
Human Factors
Our in-depth understanding of human factors ensures that your medical device design optimally accommodates the physiological and psychological needs of users through highly individualized user and validation testing.
Ergonomic Standards
We adhere to ergonomic standards to create designs that reduce user fatigue and error and improve safety.
Industry Touchstones
Our knowledge of industry-specific best practices guarantees that your medical device aligns with the highest benchmarks and regulations, including FDA and international standards.
Up-to-date Best Practices
We stay at the forefront of evolving best practices to provide innovative solutions that meet the changing demands of the healthcare industry.
Rigorous Testing for User-Centric Solutions
We ensure your medical device’s safety and user experience by conducting thorough testing using a range of prototype fidelity levels, including low, mid, and high. Our testing methods, such as A/B testing and human factors validation, leave no room for guesswork, providing rigorous validation against real user data.
By partnering with Goddard, you access a wealth of knowledge and experience that’s essential for creating safe, effective, and user-friendly medical devices.
Why Goddard?
In medical device development, challenges often include:
Tight budgets
Technological constraints
Evolving regulations
Testing and evaluation limitations
What sets us apart is our unwavering commitment to user empathy and collaboration and HFE expertise. We don’t just design for you—we design alongside you, ensuring that your medical device aligns perfectly with your vision, regulatory requirements, and user needs.
Our collaborative approach results in innovative solutions that transcend traditional boundaries, ultimately enhancing patient care and clinical workflows.
Let Us Guide Your MedTech Strategy
Navigating the complex landscape of medical device development requires a roadmap that balances regulatory compliance, design standards, and marketability.
Wondering where to consider human factors and usability engineering or where to begin designing or improving your medical technology?
We’ll work with you to strategize and ensure your medical device not only meets regulatory requirements but also sets standards for user-friendliness and market acceptance.
Already have a clear strategy in mind?
We’ll further refine your focus with a gap assessment to minimize surprises during regulatory submissions and market launches. Our expert insights can guide you toward a smoother path to success whether you’re just beginning the design process or in your nth round of validation testing.
Let’s work together to minimize risks and ensure a seamless path to success in the complex and competitive world of medical device development.
Ready to elevate your medical device design and engineering to the next level? We’re eager to embark on this journey with you.
