Solutions to Overcome Compliance, Quality and Cost in Software Development for Medical Devices
According to the World Health Organisation, there are approximately 1.5 million medical devices available in the market today, ranging from low-cost devices like the stethoscope to more expensive devices like MRI and chemotherapy machines. With the role of medical devices continuing to advance and its technology becoming more complex, understanding medical software development has never been so crucial.
Alongside John Mulcahy, CEO, HealthGenuity, Pharma IQ explores the top three challenges facing the medical device industry and provides solution summaries to help industry professionals uncover greater global market opportunities in software development while maintaining regulatory compliance.
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Other key benefits to downloading the full report:
- Gain an in-depth insight on the challenges around software development and understand how to take a more agile approach in the life-cycle development of a medical device
- Understanding how regulatory compliance can affect hardware and software of a device with some best practice suggestions for overcoming these challenges
- A deep-dive analysis on increasing market demand and competition
- Explore how the medical device industry achieve end-to-end traceability while overcoming compliance, quality and cost issues in software development
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