News & Events

Do’s and Dont’s for an FDA Visit in Your Histology Lab

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.

Store Preclinical Study Materials in Compliance with FDA Good Laboratory Practices (GLPs)

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:

Upcoming Events

ITP Course 2019

August 14-16, 2019

Indianaplis, IN

European Congress of Toxicologic Pathology

September 17-20, 2019

Cologne, Germany

Society for Neuroscience

October 19-23, 2019