Global Certificate in Pharma Quality Control Management
-- ViewingNowThe Global Certificate in Pharma Quality Control Management is a comprehensive course designed to empower learners with critical skills in ensuring drug safety and efficacy. This certificate program emphasizes the importance of quality control in pharmaceutical production, meeting the increasing industry demand for experts who can maintain high-standard manufacturing processes.
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โข Pharma Quality Control Management Fundamentals: Introduction to Quality Control (QC), its importance, and role in the pharmaceutical industry. Understanding regulatory requirements and industry standards. โข Quality Systems and Standards: Detailed study of quality systems, standards, and regulations like GMP, GLP, and GDP. Compliance requirements and best practices. โข Quality Risk Management: Risk identification, assessment, and management in pharma QC. Tools and techniques for risk analysis, like FMEA and HACCP. โข Analytical Method Validation: Basic principles, methodologies, and regulatory requirements for analytical method validation. Validation parameters, documentation, and reporting. โข Pharmaceutical Laboratory Techniques: Common laboratory techniques used in pharmaceutical QC, like chromatography, spectroscopy, and dissolution testing. โข Quality Control in Production and Manufacturing: QC practices during production and manufacturing. In-process controls, finished product testing, and documentation. โข Stability Testing and Monitoring: Understanding stability testing principles, ICH guidelines, and stability studies. Monitoring, data analysis, and reporting. โข Change Management and Continuous Improvement: Change management principles, continuous improvement strategies, and Six Sigma methodologies in QC management. โข Quality Control Data Management and Reporting: Data management best practices, documentation, and reporting in QC. Data integrity, electronic records, and signatures.
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