A guide to implement current good manufacturing practices (cGMP) and GMP standards in pharmaceutical manufacturing.
What you will learn
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Fundamentals of current Good Manufacturing Practices (cGMP) β Understand the core principles and importance of GMP in pharmaceutical and biotech industries.
Regulatory Compliance & Guidelines β Learn about FDA, WHO, EU, and ICH GMP regulations and how to meet global compliance standards.
cGMP Documentation & Record-Keeping β Master proper documentation practices to ensure regulatory approval and audit readiness.
Quality Assurance & Quality Control (QA/QC) β Gain insights into best practices for maintaining product quality and safety.
cGMP Audits & Inspections β Prepare for GMP audits by regulatory authorities and learn how to handle non-compliance issues.
Contamination Control & Cleanroom Management β Understand essential hygiene, sterilization, and contamination prevention techniques.
GMP in Manufacturing & Supply Chain β Learn how cGMP principles apply to production, packaging, labeling, and distribution.
Real-World Case Studies & Best Practices β Apply cGMP principles through real-life industry examples and case studies.
English
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