The doorbell rings and waiting at the front door are FDA inspectors... What do you do? First, welcome them in. Second... DON’T PANIC! Unless directed “For Cause”, FDA visits are routine inspections used to assess your lab’s compliance with applicable regulations and to verify the quality and integrity of your study data.
Preclinical research studies generating data for submission to the Food and Drug Administration (FDA) must adhere to Good Laboratory Practices (GLPs). These practices embody a set of principles that guide how laboratories plan, perform, monitor, document and archive study activities in an effort to enhance the quality and validity of test data. Below, you’ll find some practical tips on finding the right archiving facility for the long term storage of your study materials:
Date
March 12-26, 2021
Location
Virtual
Booth Number
Search for StageBio on the Exhibitor Page
513.204.4400
