Aging population, growth of chronic diseases, resource constraints, and the transition to value-based care will define the future of the medical devices industry. Addressing these challenges requires smart mechanical and electronics manufacturing services (EMS) and turnkey solutions that optimize production costs and bring down time-to-market.
Adopt an integrated medical device manufacturing approach for reduced costs, efficient operations, and shorter product development cycles.
Address challenges of medical device manufacturing that include obsolescence management, quality control, regulatory compliance, cost management, and faster time-to-market, while adhering to Good Manufacturing Practices (GMP).
An ISO 13485 certified design house, and mechanical, and electronics manufacturing facility under one roof enables seamless integration across your product life cycle—from design to engineering to manufacturing.
Our robust policies and processes safeguard your IPR at every stage, ensuring that your sensitive technology or proprietary data is not infringed upon.
Our broad network of ecosystem partnerships ensures that you can leverage India’s favorable policies toward medical devices and outsourced contract design, development, and manufacturing.
“We have a long-standing relationship with Cyient and are very excited to partner with them in the fight against diseases such as COVID-19. Together we endeavor to ensure that our game-changing Truenat technology reaches the frontline healthcare professionals for rapid and accurate screening at the point of care which is the need of the hour.”
“We are proud to support our customers in the healthcare industry at this critical time. We will continue to do everything we can to help reduce the impact of this crisis on our customers’ operations as they focus on delivering the technology needed to fight Covid-19 at a national and global level.”
We helped a leading medical device equipment manufacturer realize $2 million in material savings. Here’s how.
For more than 25 years, Cyient has been delivering integrated design, engineering, and manufacturing capabilities to medical device companies worldwide.
We invest in scalable manufacturing infrastructure. Our mechanical and electronics manufacturing facilities meet stringent quality standards that comply with FDA and CE Mark requirements.
We ensure that our end-products meet very robust standards in reliability, safety, and performance by complying with ISO 13485: 2016 and AS9100 standards for our facilities.
Our offerings are tailor-made to each customer’s unique requirements, delivering maximum benefit.
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