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Three FDA Initiatives That Affect Life Sciences

How the program alignment, case for quality, and transparency initiatives help healthcare

Larry Spears
Tue, 04/14/2015 - 11:45
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If you’ve been in the life science industry for awhile, you know it never gets easier but instead more complicated year after year. For example, unique device identification (UDI) requirements, combination product rules, and updated electronic medical device reporting (eMDR) requirements add to the complexity of a quality management system for good manufacturing practices (GMP) requirements.

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