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