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Study finds 62% of drug safety experts prefer AI

A new study conducted by Oracle Health Sciences and Informa Engage/Pharma Intelligence has showed that 62% of drug safety experts prefer using artificial intelligence (AI) for adverse event (AE) processing.

Introducing Morphologically Directed Raman Spectroscopy

Drug formulation, an integral step in the regulated pharmaceutical industry, involves the careful blending and processing of precisely specified and measured components to create a final product that can be administered to deliver the required clinical dose.

Risk Assessment: A Closer Look

The US Food and Drug Administration is placing heightened emphasis on risk assessment. ICH Q9, Quality Risk Management was adopted by the FDA in June 2006. 

European API Producer Providing CDMO Service

Polpharma is a European active pharmaceutical ingredient (API) producer with current good manufacturing practice (cGMP) compliant and US Food and Drug Administration (FDA) approved multipurpose facilities and provides a contract development and manufacturing organisation (CDMO) servic

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