Global Certificate in Pharmaceutical Quality Standards
-- ViewingNowThe Global Certificate in Pharmaceutical Quality Standards is a comprehensive course that equips learners with the essential skills needed to excel in the pharmaceutical industry. This course highlights the importance of quality standards in pharmaceuticals, emphasizing the significance of adhering to these standards to ensure patient safety and regulatory compliance.
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โข Pharmaceutical Quality Standards Overview: Introduction to global pharmaceutical quality standards, including definitions, purposes, and benefits. โข Regulatory Framework: Examination of international regulations and guidelines for pharmaceutical quality standards, such as ICH, WHO, and FDA. โข Quality Management Systems (QMS): Exploration of QMS principles, implementation strategies, and best practices in the pharmaceutical industry. โข Good Manufacturing Practices (GMP): Comprehensive review of cGMP, including its history, requirements, and impact on pharmaceutical manufacturing. โข Quality Risk Management (QRM): Principles and practices of QRM, focusing on ICH Q9 and its integration into the pharmaceutical quality system. โข Quality Control & Assurance: Overview of quality control and assurance principles, processes, and responsibilities. โข Pharmaceutical Validation: Introduction to the concept of validation, including process, equipment, and computerized system validation. โข Change Management: Change management principles and best practices, including impact assessment, approval, and implementation. โข Pharmaceutical Quality System Audits: Overview of internal and external audits, their objectives, and processes. โข Continuous Improvement in Pharmaceutical Quality: Implementing continuous improvement strategies and techniques in the pharmaceutical quality system.
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