Learn How Medical Device Development is Changing
Medical device development is changing. Products are becoming more complex, the FDA and other regulatory agencies require ever more stringent documentation, and more teams are contributing to the design and delivery of a product.
We conducted a survey of more than 400 engineering, R&D, testing, and regulatory professionals to gauge the state of medical device development in 2013.
This report reveals insights such as:
- Why teams are abandoning document-centric product development approaches
- What the most time-consuming tasks are, and how these tasks provide little value to development
- How teams struggle with creating and maintaining a traceability matrix
- What is preventing teams from improving their product development processes
Request your copy today and learn how medical device development is changing.
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