The medical device industry is consistently challenged to supply safe and effective solutions for the end user, considering unique patient needs and conditions.
With the development of new technologies, including biodegradable materials, cell therapy, or combination devices, the inherent variability and difficulty of standardizing testing methods exponentially increases. To address these emerging challenges, the standards community has been developing working groups comprised of industry, research, clinic, and patients to holistically evaluate how these advances affect and will affect standards.
Read the Quality Magazine article for the full story.
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