Certificate in Pharma Quality Control Audits

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The Certificate in Pharma Quality Control Audits is a comprehensive course designed to meet the growing industry demand for skilled professionals in pharmaceutical quality control. This course emphasizes the importance of implementing and maintaining quality control systems that comply with regulatory standards.

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이 과정에 대해

Learners will gain essential skills in conducting audits, identifying non-conformities, and implementing corrective actions to ensure product quality and patient safety. With the global pharmaceutical industry projected to reach $1.5 trillion by 2023, there is an increasing need for qualified professionals who can ensure compliance with regulatory standards and maintain product quality. By completing this course, learners will be equipped with the necessary skills to advance their careers in the pharmaceutical industry, providing them with a competitive edge in the job market. They will have the ability to conduct thorough audits, analyze data, and make informed decisions to improve quality control systems and ensure regulatory compliance.

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과정 세부사항


• Pharma Quality Control Audits Overview
• Regulatory Framework for Pharma Quality Control Audits
• Good Manufacturing Practices (GMP) in Pharma Audits
• Quality Management Systems (QMS) in Pharma Audits
• Risk Management in Pharma Quality Control Audits
• Documentation and Record Keeping in Pharma Audits
• Laboratory Analysis and Testing in Pharma Quality Control Audits
• Data Integrity and Analysis in Pharma Audits
• Pharma Audit Planning, Execution, and Reporting
• Corrective and Preventive Actions (CAPA) in Pharma Quality Control Audits

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