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
July 1-31, 2020
Location
https://www.toxicology.org/events/am/AM2020/exhibits.asp
Booth Number
Check our exhibit listing on the SOT Virtual Exhibit page. We missed seeing you at SOT and would like to learn how we might help you with your current and future projects. Book a meeting with us, we'll send the snacks!
513.204.4400
