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Case study of FDA warning letters
Muhammad Asim Niazi
January 23, 2024
A warning letter is a part of communication by the FDA with the manufacturer to share their finding to remove the discrepancy found during their inspection and inform the status of the manufacturer's measures.
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FDA sends four warning letters for cGMP violations
europeanpharmaceuticalreview
April 08, 2019
The US Food and Drug Administration has posted warning letters to four companies who produce homeopathic drug products for significant violations of current good manufacturing practice (cGMP) regulations…
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Summary of Warning Letters Issued by FDA in 2018 Q1
zhulikou431
April 08, 2018
FDA issued 17 warning letters on production quality (including 6 in January, 7 in February, and 4 in March) in 2018 Q1
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Analysis of Warning Letters Issued by FDA in 2018 Q1
zhulikou431
April 08, 2018
Situation of Strict Regulation of Pharmaceutical Agencies Stays Unchanged
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Data Analysis of Relevant Warning Letters of FDA on Computer System
en-cphi.cn
June 30, 2017
As is known to all, FDA, one of the strictest drug administration agencies in the world, mainly take charge of safeguarding the health and safety of consumers based on federal food, drug, cosmetics laws and other laws.