Improve Your GMP Compliance With Innovative Employee Training: Nine Small-Group Exercises That Work
Product Details
Could a small change in how you train employees make a huge difference in boosting quality and avoiding costly FDA warning letters and Form 483s?
Absolutely! “Insufficient training” is frequently cited by inspectors. Now, an innovative small-group approach helps you defuse this trigger so your odds of sailing through inspections soar. And when every member of your workforce actively applies SOPs and GMPs to their own real-world situations, you will see quality soar too.
Better yet, this innovative small-group approach can deliver these results even as your training budget shrinks.
Here’s how to get on board …
Small-Group Training Makes Make Big Improvements in Compliance
Need to boost compliance with SOPs and FDA regulations? Need to make those improvements fast and on a tight budget?
Regulatory training expert Barbara Immel says the key is to trade old training methods for nine small-group training exercises that can deliver immediate compliance — and quality — breakthroughs for companies of all sizes.
In this 90-minute audio CD/Transcript, you’ll learn how to use nine highly effective small-group learning experiences to engage your workforce in applying regulations and guidance documents to real-world situations. In addition, you’ll learn how to choose which of the nine exercises will have the biggest impact for your firm — and how to measure success.
Order now for your entire team to turbo-charge compliance training and learn how to:
- Leverage small-group exercises for maximum retention and application of learning
- Engage everyone in brainstorming where and how to improve
- Prepare for the most difficult FDA questions — before inspectors arrive
- Use other firms’ warning letters to spot and fix similar compliance issues in your own operation
- Turn the FDA’s inspection manual into your own troubleshooting checklist
- Create highly effective GMP review sessions that get everyone involved
- Identify potential SOP problems — before inspectors can cite them
- Review and implement ICH guidelines on stability
- Conduct mock failure investigations to drive out weak links
- Manufacture fake “products” following cGMPs
As an attendee, you’ll also receive two complimentary best-practice white papers on training.