FDAzilla The Leading Platform for GMP Inspection Analytics
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The FDAzilla family of products unlocks regulatory insights and reduces risk for FDA regulated businesses. Expert Guidance from Barb Unger. Read the Medical Device Blog. Week of Mar 4th 2018 FDA Sent These Warning Letters to Pharma Companies. CGMP Quality Assurance and FDA 483s. 74 New FDA 483s March 15th 2018.
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The process of approving these medical devices is flawed according to the Institute of Medicine. All clinical trials must report.
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FDAzilla The Leading Platform for GMP Inspection AnalyticsDESCRIPTION
FDAzilla provides actionable information on FDA-regulated companies to pharmaceutical, medical device, food, financial professional services companies.PARSED CONTENT
The web page fdazilla.com had the following in the web site, "The FDAzilla family of products unlocks regulatory insights and reduces risk for FDA regulated businesses." I saw that the website stated " This is a transformative tool." They also said " You are taking the FDAs data and making it actionable. Built by data scientists for GMP quality professionals and service firms, FDAzilla is the leading platform for GMP inspection analytics. Sign up for a demo. Data Integrity The Whole Story. China Drug Inspections, 2016. 10 Ways to Prep for a GMP Inspection. Sign up for a demo."SEE SUBSEQUENT WEBSITES
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