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  Managing evolving requirements to improve medical device design

  Managing evolving requirements is a core competency for medical device technical specifications and understanding health care end users.

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  When should you use Open Source Software in Medical Devices?

  Open Source Software Medical Devices: Using OSS libraries within a Software System of a Medical Device or In Vitro Diagnostic Device.

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  3D Printed Medical Devices – Insight into the FDA Guidance on Additive Manufacturing

  FDA Guidance on Additive Manufacturing (AM) – offers new ways to integrate parts not only for prototypes, but for final products.

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  Comparing Consumer and Medical Design Control

  Why design control is required for medical devices and is superfluous in the consumer goods design with advantages and disadvantages.

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  Avoid these 11 costly medical device development mistakes

  11 medical device development mistakes that surfaced frequently in a variety of products.  Avoid them to reduce cost and time to market.

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  Cellular reprogramming for medical applications

  Cellular reprogramming is a strategy for a variety of medical applications where an adult cell is flipped from one type directly into another.

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  Determining the best method to detect E. coli

  When selecting a method for developing an assay, whether it is for detecting bacteria or simulating fluid, the approach all depends on…

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  Medical Devices and GDPR (the EU General Data Protection Regulation)

  GDPR is designed to enhance the privacy and security of data subjects.  Medical devices and GDPR cross paths in many areas.

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  Medtech resolutions for 2018

  Our employees’ medtech resolutions include great ideas.  What are your improvement plans?  We’d love to hear and share them.

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