Envisage partners with US-based medical device companies to design, validate, and scale life-saving technologies. From diagnostic platforms to therapeutic and surgical devices, we provide end-to-end engineering and staffing solutions that ensure safety, compliance, and innovation at every stage of development.
Meeting stringent FDA, ISO, and global compliance standards
Ensuring reliability and performance of diagnostic and therapeutic systems
Accelerating time-to-market while maintaining safety and quality
Accessing specialized engineering expertise in hardware, software, and validation
Hardware, firmware, embedded software, and mechanical systems design
Comprehensive verification, compliance, and regulatory documentation
Specialized engineers, QA professionals, and domain experts for medical device R&D
From early-stage prototyping to commercial rollout and post-market sustenance
We deliver complex projects through global collaboration, blending onshore precision with offshore efficiency for faster timelines, reduced costs and superior results.
Our flexible staffing approach, backed by an extensive talent network, is dedicated to quickly deploying the right expertise to fulfill evolving client requirements and strategic goals.
Our consulting-driven approach, powered by deep technology and business insights, is dedicated to guiding clients toward optimized processes, innovative solutions and sustainable growth outcomes.
Complete our NDA-secured contact form, choose a convenient time, and schedule a Zoom session with our expert team.
Discuss your vision with our specialists to assess its technical feasibility and potential for successful implementation.
We prepare a detailed proposal outlining budget, timeline, and scope—tailored to your specific project requirements.
With the agreement in place, we assemble a multi-disciplinary team to initiate and drive your project forward.