Advanced Good Manufacturing Practice (GMP) for the Pharmaceutical Industry

Categories: GMP and GLP
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About Course

Enhance your knowledge of pharmaceutical Good Manufacturing Practice (GMP) based on international regulatory expectations. This course covers advanced GMP principles, quality systems, documentation, contamination control, production, validation principles, risk management principles, data integrity, and inspection readiness. It is designed for pharmaceutical professionals who want to strengthen compliance, improve operational excellence, and prepare for regulatory inspections.

What Will You Learn?

  • Understand advanced GMP principles and regulatory expectations.
  • Interpret WHO, EU, FDA, PIC/S, and ICH GMP requirements.
  • Implement an effective Pharmaceutical Quality System.
  • Improve Good Documentation Practices (GDP).
  • Reduce deviations through effective GMP implementation.
  • Apply Quality Risk Management tools.
  • Understand Data Integrity requirements.
  • Prepare for GMP inspections.
  • Improve inspection readiness.
  • Strengthen contamination control practices.
  • Understand validation and qualification concepts.
  • Improve cross-functional GMP compliance.
  • Apply GMP knowledge to real pharmaceutical situations.

Course Content

Day 1: Advanced GMP Fundamentals

Day 2: Production operations

Day 3: Quality Control, Documentation, Data Integrity

Day 4: GMP Audits & Inspection Readiness

Additional Module: Validation and Qualification