Medical Technology Industry: Increasingly Complex, Costly and Competitive
Global demand for high-quality medical systems is driving manufacturing expansion into emerging markets. This shift presents opportunity and growth as well as increased cost and risk. Specific challenges are presented to those companies moving into new markets such as fragmented global regulatory compliance, foreign localization and FDA manufacturing and design specifications. Navigating through the various regulatory standards, such as ISO 62366 and IEC 62304, can be a challenge to any vendor creating new Class II and Class III medical devices. ICS understands these larger issues and the impact they may have on your medical device development.
What We Do
We design and build great products, period.
ICS partners with medical technology organizations to manage development complexity and stabilize new product introductions. We also work with engineers to reduce redundancies, costs and enhance software performance to provide intelligent products to increasingly diverse markets.
What We Offer
Custom Client Engagements
Learn about how ICS provides high quality, stable and cost-effective medical systems for diverse markets.