Executive Development Programme in Pharma Quality Control Audits

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The 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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By enrolling in this course, learners will develop a solid understanding of the latest auditing techniques, regulatory requirements, and quality management systems specific to pharmaceutical manufacturing. They will gain practical experience in conducting mock audits, analyzing data, and preparing audit reports. Upon completion, learners will be equipped with essential skills for career advancement in quality control, auditing, and regulatory affairs roles within the pharmaceutical industry. This programme not only enhances learners' professional expertise but also provides a competitive edge in the job market, making it an excellent investment for career growth and development.

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ใ‚ณใƒผใ‚น่ฉณ็ดฐ

โ€ข Pharma Quality Control Audits Fundamentals: Understanding the basics of Pharma Quality Control Audits, including its importance, objectives, and benefits.
โ€ข Regulatory Framework: An overview of the regulatory bodies and their guidelines, such as FDA, EMA, and ICH, that govern Pharma Quality Control Audits.
โ€ข Quality Management System (QMS): Principles and best practices of QMS, and its role in ensuring compliance with regulatory requirements.
โ€ข Good Manufacturing Practices (GMP): Understanding the GMP regulations, compliance requirements, and its impact on Pharma Quality Control Audits.
โ€ข Risk Management: Techniques for identifying, assessing, and controlling risks in Pharma Quality Control Audits.
โ€ข Data Integrity: Best practices for ensuring data integrity in Pharma Quality Control Audits, including data collection, storage, and reporting.
โ€ข Audit Planning and Execution: Steps and techniques for planning and executing Pharma Quality Control Audits, including documentation, communication, and reporting.
โ€ข Audit Findings and Reporting: Techniques for analyzing and reporting audit findings, including writing effective reports, communicating results, and implementing corrective actions.
โ€ข Continuous Improvement: Strategies for using Pharma Quality Control Audits to drive continuous improvement in organizational processes and performance.

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ใ‚ตใƒณใƒ—ใƒซ่จผๆ˜Žๆ›ธใฎ่ƒŒๆ™ฏ
EXECUTIVE DEVELOPMENT PROGRAMME IN PHARMA QUALITY CONTROL AUDITS
ใซๆŽˆไธŽใ•ใ‚Œใพใ™
ๅญฆ็ฟ’่€…ๅ
ใงใƒ—ใƒญใ‚ฐใƒฉใƒ ใ‚’ๅฎŒไบ†ใ—ใŸไบบ
London College of Foreign Trade (LCFT)
ๆŽˆไธŽๆ—ฅ
05 May 2025
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