Medical Devices and Equipment

Overview

Our medical device design services offers concept development, product designing, prototype development, value engineering and obsolescence management to ensure fast-paced market launch and compliance to ISO:13485 guidelines and excellent at meeting regulatory-compliant medical device design processes. Our processes also include maintaining Device Master Files (DMR) to support in regulatory compliance and to easily identify source of error under situations of any non compliance as per FDA. Our medical device team addresses the whole development process from systems, software, electronics, mechanical, quality assurance and regulatory compliance. We can help you optimize your budget and shorten development times of Class l, ll, or lll device using the latest CAD, CAE tools and technologies by our medical device engineers as per FDA, EU and Country specific guidelines.