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However, countries around the globe are at various stages of development for their regulatory policies. It can be overwhelming to know where to start to address nitrosamine impurities in drug products. Before the COVID pandemic, industry issues like this were often dealt with in a silo.
Paradigm Shift in DrugDevelopment: Analytical Quality by Design and Analytical Procedure Life Cycle In today’s pharmaceuticalmanufacturing environment, companies face increasing pressure to respond to changing demands across the global medicines supply chain while still maintaining the quality of their drug products.
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