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; we blend onshore control with offshore efficiency for faster timelines, reduced costs and desired outcomes.
Backed by a deep talent network, our flexible staffing model quickly matches the right expertise to evolving client needs and strategic goals.
Our consulting-driven approach combines deep technology and business insight to help clients optimize processes, drive innovation, and achieve sustainable growth.
Reach out to us via the contact form to get started. We’ll then share an NDA for completion, after which you can select a convenient time and schedule a Zoom session with our expert team.
Discuss your vision with our specialists to assess technical feasibility and potential for successful implementation.
We will create a detailed proposal tailored to your specific needs.
With the agreement in place, we assemble the right team to initiate and drive your project to completion.