Promoting medical innovation through medical device design

Regulatory environment
As the industry continues to innovate and leak new technologies, it is also plagued by a rigorous and ever-changing regulatory environment. Healthcare organizations are constantly looking for ways to improve clinical trials of medical devices and use breakthrough technologies to meet the growing needs of patients, healthcare practitioners, while meeting equipment guidelines and regulatory requirements. In addition, monitoring device mobility, connectivity and portability have increased, and medical device manufacturers are looking to establish cost-effective and cutting-edge connectivity services.

Embrace IT solutions
Healthcare policy reforms and technological advances have been integrated to drive the demand for new and innovative medical devices in hospitals, healthcare facilities, laboratories and governments. However, as growth poses significant challenges [and opportunities] - IT solutions can help as guidelines and tasks continue to evolve and the way medical devices are rolled out.

• Effectively manage compliance issues, as well as customer service and complaint issues
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  • Improve product development and manufacturing processes in key operational functions to meet increasingly stringent regulatory environmental requirements
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  • Minimize product development and research costs while reducing time to market
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  • Achieve superior R&D activities to ensure richer equipment [and healthcare] results
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  • Leverage cutting-edge compliance management strategies, sales and marketing analytics, and on-site services that span clinical development and production challenges

Intelligent engineering to improve health care outcomes
Intelligent engineering is the latest wave of engineering processes that enable manufacturers to drive innovation in product development:
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  • With intelligent engineering, manufacturers can easily and quickly verify error-prone features early in product development
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  • Through this type of verification, manufacturers can significantly reduce costs and speed time to market
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  • Task automation can greatly increase productivity and proactively reduce risk to help ensure a safe and reliable product
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  • Intelligent engineering delivers robust product design and delivers high quality products to patients and healthcare providers at a reasonable price
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  • Predictable output can be generated during the manufacturing process through intelligent data collection during the design phase
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  • Manufacturers can perform extensive validation of changes prior to implementation and build safer products with predictable revenue
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  • Intelligent Engineering combines model-based development, embedded hardware and firmware design, integration and test automation
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  • Device manufacturers can build connected ecosystems using medical-grade communication technologies and protocols
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  • Application development and maintenance of medical device design services to help build electronic medical records and personal health records [PHR]
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  • Infrastructure Management Services enable manufacturers to host solutions on the cloud and take advantage of remote management
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  • Finally, quality assurance and regulatory services ensure accurate product validation, certification and submission to improve health management

Become a winner
The dynamic nature of the healthcare industry is putting constant pressure on medical device manufacturers to continuously develop products that improve clinical outcomes and patient health. Capable of adapting to industry trends and rapid changes and delivering unparalleled performance, device manufacturers focused on clinical outcomes and reduced support costs will be winners and future leaders.

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