FDA mandates regarding Good Laboratory Practices (GLP) have been around since the 1970s when the regulations were finalized. However, GLP deficiencies are still routinely cited during regulatory inspections. An understanding of the origins of GLP, plus utilizing proven inspection preparation steps, can help to strengthen GLP programs resulting in compliant operations. This 90-minute course will provide you with the tools to understand proper conduct of GLP studies, safeguard against inspection deficiencies, and satisfy regulatory agencies that your efforts are compliant.
By attending this course, you will learn:
- History and background of GLP regulations
- Actionable steps that will allow you to be prepared for ANY contingency
- Tips & tricks to prepare for – and survive – a FDA GLP inspection
- The top issues inspectors look for and how to avoid them