Certificate in Pharmaceutical Analysis: Quality Assurance
-- ViewingNowThe Certificate in Pharmaceutical Analysis: Quality Assurance is a comprehensive course designed to equip learners with critical skills in the pharmaceutical industry. This program emphasizes the importance of quality assurance in pharmaceutical analysis, focusing on regulatory compliance, lab techniques, and data interpretation.
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⢠Introduction to Pharmaceutical Analysis: Fundamentals of pharmaceutical analysis, analytical techniques, and their applications in quality assurance.
⢠Quality Assurance Concepts: Quality assurance principles, regulatory framework, and good laboratory practices in pharmaceutical analysis.
⢠Chromatographic Techniques: Theory and practical applications of thin-layer chromatography (TLC), high-performance liquid chromatography (HPLC), and gas chromatography (GC) in pharmaceutical analysis.
⢠Spectroscopic Techniques: Overview of UV-Vis, FT-IR, and NMR spectroscopy, with a focus on their role in pharmaceutical analysis and quality control.
⢠Pharmaceutical Dosage Form Analysis: Analysis of solid, liquid, and semi-solid dosage forms, including tablet friability, disintegration, and dissolution testing.
⢠Validation Methods: ICH guidelines for method validation, including accuracy, precision, specificity, detection limits, and robustness.
⢠Stability Testing: Stability testing principles, International Conference on Harmonisation (ICH) guidelines, and stress testing.
⢠Data Analysis and Report Writing: Statistical analysis of data, interpretation of results, and report writing in pharmaceutical analysis.
⢠Regulatory Affairs: Overview of regulatory affairs, including submissions, approvals, and labeling requirements.
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