Greetings!
GMP compliance is often tested in the details.
An incomplete record. A deviation that was not properly investigated. An outdated SOP. Inconsistent training. A change that was implemented without adequate control.
Individually, these may seem manageable. During an inspection, they can point to much larger weaknesses in a pharmaceutical quality system.
This practical workshop takes a closer look at GMP in day-to-day pharmaceutical operations, helping you understand how to:
- Build stronger quality control and quality assurance practices
- Develop effective SOPs and maintain accurate GMP documentation
- Investigate deviations and out-of-specification results
- Strengthen production controls, validation, and change control
- Establish effective training and sanitation programs
- Prepare your people, documentation, and systems for inspectors and auditors
You’ll explore not only the core requirements of GMP, but how those requirements translate into the systems, records, controls, and practices regulators expect organizations to demonstrate consistently. Whether you work in QA, regulatory affairs, manufacturing, documentation, product development, or another regulated function, this workshop provides a practical framework for strengthening compliance and protecting product quality.
*All participants will receive a Certificate of Attendance upon completion. |
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