Professional Certificate in GMP and Pharma Supplies

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The Professional Certificate in GMP & Pharma Supplies is a comprehensive course that provides learners with a solid understanding of Good Manufacturing Practices (GMP) and pharmaceutical supplies. This course is crucial in the pharmaceutical industry, where adherence to GMP ensures the production of high-quality drugs, reducing risks to patient health.

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With the increasing demand for qualified professionals in the pharmaceutical sector, this course equips learners with essential skills to advance their careers. Learners gain in-depth knowledge of GMP principles, quality control strategies, and pharmaceutical supply chain management. They also learn to navigate regulatory requirements, ensuring compliance and maintaining the highest industry standards. Upon completion, learners will be able to demonstrate their expertise in GMP and pharmaceutical supplies, making them attractive candidates for various roles in the industry. This course is an excellent opportunity for professionals seeking to enhance their skillset and expand their career opportunities in the rapidly growing pharmaceutical sector.

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โ€ข Introduction to GMP (Good Manufacturing Practices): An overview of GMP principles, regulations, and their importance in pharmaceutical manufacturing.
โ€ข Quality Control and Quality Assurance: Understanding the role of QC and QA in GMP, including quality risk management, documentation, and change control.
โ€ข Facility and Equipment Management: Best practices for maintaining and managing facilities and equipment to ensure GMP compliance.
โ€ข Material Management and Supply Chain: Procurement, storage, and handling of raw materials, components, and packaging materials, focusing on supplier qualification and supply chain integrity.
โ€ข Production Processes and Controls: Designing, implementing, and monitoring production processes, including in-process controls, to ensure consistent product quality.
โ€ข Laboratory Controls: Method validation, analytical testing, and laboratory record management in support of GMP compliance.
โ€ข Packaging and Labeling: Requirements for pharmaceutical packaging and labeling, including serialization and tamper-evident features.
โ€ข Complaint Handling and Product Recall: Establishing procedures for handling customer complaints, conducting investigations, and implementing corrective actions, as well as managing product recalls when necessary.
โ€ข Regulatory Inspections and Audits: Preparing for and managing regulatory inspections and audits, including self-inspections and mock inspections.

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ใ‚ตใƒณใƒ—ใƒซ่จผๆ˜Žๆ›ธใฎ่ƒŒๆ™ฏ
PROFESSIONAL CERTIFICATE IN GMP AND PHARMA SUPPLIES
ใซๆŽˆไธŽใ•ใ‚Œใพใ™
ๅญฆ็ฟ’่€…ๅ
ใงใƒ—ใƒญใ‚ฐใƒฉใƒ ใ‚’ๅฎŒไบ†ใ—ใŸไบบ
London School of International Business (LSIB)
ๆŽˆไธŽๆ—ฅ
05 May 2025
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