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Beyond Compliance: Connecting the Dots Between Quality, Engineering, and Regulatory

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w_dasa30c.gif To be successful, medical device companies continually need to produce innovative products that are clinically and economically relevant.

In an effort to accelerate the delivery of innovative, safe, and fully compliant medical devices, companies:
  • Strive to provide additional solutions to enhance the patient experience and address patient unmet needs
  • Reduce both time-to-market and development costs
  • Increase outsourcing and externalization
When certain issues hinder innovation, it’s crucial to understand the type of solution that promotes collaborating to accelerate design and meet long-term business goals. Uncover how teams can focus on quality, accelerate innovation, and improve operational efficiency while ensuring global regulatory compliance.

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