Professional Certificate in PharmaTech Quality Management Systems

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The Professional Certificate in PharmaTech Quality Management Systems is a comprehensive course designed to meet the growing industry demand for skilled professionals in pharmaceutical quality management. This certificate course emphasizes the importance of implementing robust quality systems to ensure compliance with regulatory standards and produce high-quality pharmaceutical products.

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By enrolling in this course, learners will gain essential skills in process validation, quality risk management, change management, and continuous improvement. These skills are vital for career advancement in the pharmaceutical industry, where regulatory compliance and quality assurance are paramount. Upon completion of the course, learners will be equipped with the knowledge and skills to develop, implement, and maintain quality management systems that meet international regulatory standards. This certificate course is an excellent opportunity for professionals seeking to enhance their career prospects in the pharmaceutical industry and contribute to the development of safe and effective pharmaceutical products.

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โ€ข Quality Management Systems Overview: Introduction to PharmaTech Quality Management Systems, key concepts, and benefits.
โ€ข Quality Management System Standards: Overview of industry standards such as ISO 9001, ISO 13485, and 21 CFR Part 820.
โ€ข Quality Policy and Objectives: Developing and implementing quality policies and objectives to drive continuous improvement.
โ€ข Quality Documentation: Creating, maintaining, and controlling quality records, including Standard Operating Procedures (SOPs), work instructions, and quality plans.
โ€ข Quality Risk Management: Identifying, assessing, and controlling risks to ensure compliance and patient safety.
โ€ข Change Management: Managing changes to the quality management system, processes, and products.
โ€ข Quality Audits and Inspections: Preparing for, conducting, and responding to internal and external audits and inspections.
โ€ข Continuous Improvement: Implementing a culture of continuous improvement through data analysis, corrective and preventive action (CAPA), and trend analysis.
โ€ข Supplier Management: Evaluating, selecting, and monitoring suppliers to ensure compliance and product quality.

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PROFESSIONAL CERTIFICATE IN PHARMATECH QUALITY MANAGEMENT SYSTEMS
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London College of Foreign Trade (LCFT)
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05 May 2025
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