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Good Manufacturing Practices [cGMP]

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10,000.00 LE 10000.0 EGP 10,000.00 LE

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Description

This introductory cGMP course is designed especially for new graduates, entry-level professionals, and individuals starting their career in the pharmaceutical, food, chemical, 1ry packaging and cosmetics industries.

The course provides a simplified, practical overview of Good Manufacturing Practices (GMP) — the international standard that ensures products are consistently produced and controlled according to quality requirements.

Through real examples from manufacturing sites, trainees learn the essential foundations of working in a GMP environment, including hygiene, documentation, production behavior, contamination prevention, and basic quality concepts.

The course is delivered in an easy-to-understand format, helping beginners build the confidence and readiness needed to join the industry.

By the end of this course, participants will be able to:

  • Understand what GMP is and why it is essential for product quality and patient safety.
  • Recognize the basic structure of a pharmaceutical quality system.
  • Follow correct documentation practices (ALCOA+).
  • Undestand good laboratory practices GLP
  • Apply basic hygiene, gowning, and workplace discipline rules.
  • Identify sources of contamination and how to prevent them.
  • Understand equipment basics, cleanroom behavior, and production workflow.
  • Become job-ready for QA, QC, production, and supply chain roles.

Who Should Attend

This intro-level course is perfect for:

  • Fresh graduates from Pharmacy, Science, Biotechnology, Engineering, Agriculture
  • Entry-level applicants seeking their first job in pharma or food factories
  • Interns and trainees preparing for interviews or on-site training
  • Anyone who wants to understand GMP basics before joining the industry

Key Takeaways

  • Flexible Attendance Options – Join in-person at VALOR or virtually through our live interactive platform.
  • Recorded Sessions – Enjoy limited access to recordings for three months after course completion for review and reinforcement.
  • Repeat for Free – Participants may re-attend inperson any future round of the same course at no additional cost.
  • Accredited Certificate – Receive a QR-coded certificate for authenticity verification and professional recognition.
  • Comprehensive Resources – Access digital materials, trainer support, and post-course assessments through VALOR’s e-learning platform. 

Course Topics

• Quality Systems ( QMS, GDP, Deviation management, Change control, supplier qualification, APR)

• Laboratory Systems (  Compendia, Specifications,  Sampling, record-keeping,   Instrument handling,  Stability programs, OOS)

• Infrastructure: Facilities, Utilities, Equipment

• Materials & Distribution management

• Manufacturing , Filling, Packaging& Labeling Systems

• Product Development

Number Of Sessions

10 Sessions