Pharmaceutical Analysis and Quality Assurance

Pharmaceutical analysis and quality assurance are essential for maintaining the safety, efficacy, and consistency of pharmaceutical products. This session focuses on advanced analytical techniques including HPLC, UPLC, GC, LC–MS/MS, NMR, FTIR, and UV–Visible spectroscopy, along with method development and validation as per ICH guidelines. Topics include impurity profiling, stability and degradation studies, bioanalytical method development, and quality control testing of raw materials, intermediates, and finished dosage forms. The session also addresses pharmaceutical quality systems, GMP compliance, data integrity, regulatory requirements, and emerging trends such as automation, digitalization, and real-time quality monitoring in pharmaceutical analysis.

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