Control limit of Nitrosamines and N-nitroso compounds
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2
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285
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July 8, 2024
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On the role of digital tools in nitrosamine risk assessment for drug substance and drug product manufacturing processes -Pub
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0
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141
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June 13, 2024
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π°π· Case study on the Occurrence of Impurities in Pharmaceuticals (Focusing on NDMA Cases)
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0
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211
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May 31, 2024
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πͺπΊ EDQM - top 10 deficiencies observed in new CEP applications
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0
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825
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March 14, 2024
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πΊπΈ FDA CDER Generic Drug Forum (GDF) 2024
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5
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1191
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April 14, 2024
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Identifying the Risk of Formation of Nitrosamines and Other Potentially Mutagenic Impurities during API Manufacture Using In Silico Risk Assessment -Pub
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0
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1129
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June 6, 2023
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Nitrosamine Risk Assessments in Oligonucleotides
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2
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586
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August 10, 2023
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