With over 35,000 global associates, our Engineering First approach, and unmatched domain expertise, we’re the verification and validation experts for renowned companies like Medtronic, J&J MedTech, and more, in collaboration with our partners at IZiel. Experience V&V excellence with Virtusa's comprehensive, automated, and tailored solutions. With over 400+ domain-trained test professionals in healthcare and life sciences, we are known for delivering top-notch verification and validation services that enhance your product quality, reduce time to market, and ensure regulatory compliance.
In a world filled with regulations and ever-changing guidelines, launching defect-free products while staying compliant can feel like navigating a maze.
From consulting to scaling, our Engineering First approach ensures we bring the right domain expertise, rigorous verification and validation, and cutting-edge test automation capabilities to the table. We're here to improve your product quality documentation, reduce time to market, and make the complex simple. FDA QSR 21 CFR Part 820, ISO 13485, IEC 62304, and more are no challenges for our engineering prowess.
With our help, you can successfully tackle everything from cyber security compliance to groundbreaking AR/AI surgical navigation systems, IOT-enabled pain management solutions, and even rapid test automation for home dialysis devices.
We understand the ever-evolving landscape of the medical device industry.
That's why we've created a groundbreaking verification and validation solution that addresses the challenges faced by industry leaders like you. Challenges like:
- Process change
With the adoption of agile methodologies and continuous testing, traditional V&V approaches fall short. Our solution adapts to changing processes, ensuring seamless integration and improved efficiency. - NextGen tools
Advances in AI, partner solutions, and emerging technologies demand a comprehensive approach to V&V. We offer a holistic solution that embraces the power of NextGen tools, propelling your products forward. - Complex product ecosystem
The rise of interconnected devices and diverse applications calls for a better V&V strategy. Our expertise in handling complex ecosystems ensures compliance and cost optimization. - Rise of non-functional testing
Cloud adoption and cybersecurity risks require enhanced non-functional testing. Our V&V offering covers comprehensive testing to fortify device performance and security. - Regulatory landscape
From MDD to MDR transition and evolving guidelines, staying compliant is vital. We align our V&V solution with regulatory requirements, guiding you through the ever-changing landscape.
Our Verification and Validation (V&V) solution at Virtusa empowers you with excellence in every aspect of your medical device development process.
Comprehensive testing coverage
From initial design to post-market surveillance, our solution ensures comprehensive testing coverage throughout the entire product lifecycle.
Domain expertise
With our Engineering First approach, we bring deep domain expertise to the table. Our team of experts understands the intricacies of the medical device industry, ensuring precise verification and validation aligned with regulatory requirements.
Compliance assurance
Our solution adheres to industry best practices and regulatory standards such as FDA QSR 21 CFR Part 820, ISO 13485, IEC 62304, and more.
Advanced test automation
Harnessing the power of automation, we enable efficient and reliable testing. Our state-of-the-art functional and non-functional test automation capabilities accelerate the verification and validation processes, saving time and reducing costs.
Tailored solutions
Our V&V solution is highly customizable to fit your specific workflows and systems. Seamlessly integrating with your existing infrastructure, our solution enables a smooth transition and maximizes value.
Scalability and future-readiness
In a rapidly evolving industry, scalability and future readiness are essential. Our validated assets and accelerators are designed to scale your organization's growth and accommodate future enhancements and updates, keeping you agile and ahead of the curve.
Enhance your product quality, reduce time to market, and ensure regulatory compliance with Virtusa's comprehensive Verification and Validation solution.
IZiel Healthcare is a global engineering and regulatory services provider founded in 2007. They work with major companies like Medtronic and Mediso Imaging, offering expertise in DHF, Engineering Documentation, Process Validation, QMS, and Regulatory Projects. With offices in the USA and India, IZiel's engineers are trained in Design for Six Sigma - Black Belt Level. Teaming up with Virtusa, they provide comprehensive support for software product development and the launch of connected medical devices and SaMDs in the US, Europe, and Asia.