Introduction
Who doesn’t want their business or product manufacturing unit to function with great performance? What if you could be the star manager of these units? This is not a clickbait!
Our 2-days long GMP training will equip you to increase your efficiency and strengthen your skills for a stellar career in the industry. Whether you want to level up your designation or become an entrepreneur, the credibility of a GMP course will only add stars to your portfolio.
Course Overview
For any professional working in the laboratory, it is essential to know the basic regulations and code of conduct. Good manufacturing practices comprise these regulations associated with every aspect at an operational level.
Our GMP training stretched over 2 days is curated in a beginner-friendly format. Here are some takeaways from the GMP training for employees:
- Basic regulatory norms and their benefits
- GMP in the pharmaceutical industry
- Makes the candidate familiar with technical terms and their relevance
- Training for QC labs
- Clarification on techniques to adhere to the regulations
- Norms related to design and utilities
- Good laboratory practices including equipment and instrumentation norms
Furthermore, a detailed list of topics discussed in the GMP training for pharmaceutical industry includes:
- An Introduction to Good Manufacturing Practice (GMP),
- CFR Title 21, Parts 58, 210, 211 Overview
- GMP in the Warehouse,
- Quality Control Laboratory Design
- Microbiology in the Workplace,
- Cleaning and Sanitation,
- Good Documentation Practices - GMP Laboratory
- Documentation and Record Keeping, Stability & Training
- Contamination Control,
- Production Controls,
- Packaging Controls,
- Quality Assurance and Quality Control
- Pharmaceutical’s Corrective Actions and Preventative Actions (CAPAs).
- The Regulatory Inspection
- Deviations / Non-conformances
- OOS / OOT
- How to write an effective investigation
If you are curious to know how this training is relevant to you, the following section will include the details.
Course Provider
Ms Kelly Thomas,
Vice President ,
Stallergenes GreerMs. Thomas has over two decades of cGMP hands-on industry experience in both pharmaceutical and medical device manufacturing operations. Her experience covers all Quality Systems; as well as, all areas of validation; including, process/product validation, facilities validation, CSV and 21 CFR Part 11, test method validation, equipment/automated processes and cleaning validation.
Utilizing strategic thinking, risk based approaches, and Lean principles, she has demonstrated success in steering and managing complex projects within the pharmaceutical and medical device industries.
