On November 23, 2016, the Food and Drug
Administration (FDA) published a revised draft guidance for Submission of
Quality Metrics Data. The guidance includes significant changes to the earlier
quality metrics draft guidance issued by the agency on July 28, 2015.
FDA's Quality Metrics Initiative,
announced in April 2013, encourages pharmaceutical firms to embrace continuous
improvement and foster a culture of quality by collecting and reporting
manufacturing quality data. During the comment period for the 2015 draft
guidance, manufacturers acknowledged that the initiative has the potential to
transform the way the pharmaceutical industry approaches overall product
quality and the reliability of the supply chain. However, manufacturers and
participants in ISPE’s Wave 2 Quality Metrics Pilot Program, conducted across
28 companies (83 sites, 60 products), expressed concerns over lack of clarity
regarding implementation, timelines, definitions, and evaluation guidelines.
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Posted by Dr. Tim Sandle
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