Executive Development Programme in Pharma Quality Control Audits
-- ViewingNowThe Executive Development Programme in Pharma Quality Control Audits is a comprehensive certificate course designed to meet the growing industry demand for skilled professionals. This programme emphasizes the importance of quality control audits in the pharmaceutical industry, where maintaining high standards is critical for consumer safety and regulatory compliance.
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⢠Pharma Quality Control Audits Fundamentals: Understanding the basics of Pharma Quality Control Audits, including its importance, objectives, and benefits.
⢠Regulatory Framework: An overview of the regulatory bodies and their guidelines, such as FDA, EMA, and ICH, that govern Pharma Quality Control Audits.
⢠Quality Management System (QMS): Principles and best practices of QMS, and its role in ensuring compliance with regulatory requirements.
⢠Good Manufacturing Practices (GMP): Understanding the GMP regulations, compliance requirements, and its impact on Pharma Quality Control Audits.
⢠Risk Management: Techniques for identifying, assessing, and controlling risks in Pharma Quality Control Audits.
⢠Data Integrity: Best practices for ensuring data integrity in Pharma Quality Control Audits, including data collection, storage, and reporting.
⢠Audit Planning and Execution: Steps and techniques for planning and executing Pharma Quality Control Audits, including documentation, communication, and reporting.
⢠Audit Findings and Reporting: Techniques for analyzing and reporting audit findings, including writing effective reports, communicating results, and implementing corrective actions.
⢠Continuous Improvement: Strategies for using Pharma Quality Control Audits to drive continuous improvement in organizational processes and performance.
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