GxP and Regulatory Series

The GxP and Regulatory Series provides a comprehensive view of good clinical practices and regulatory guidelines within the pharmaceutical and biotech industry.  Courses in this series provide insight on electronic signatures and records, clinical research and applied statistics, and adverse event reporting.  In addition, this series provides detailed information on good clinical, laboratory, and manufacturing practices.

View a brief demonstration highlighting the below courses within this series.

21 CFR Part 11

GCP2: Good Clinical Practice Level 2

Biostatistics

GLPO: Good Laboratory Practice Overview

Drug Safety: Adverse Event Reporting

GMPO: Good Manufacturing Practice Overview

GCP1: Good Clinical Practice Level 1

GxP Industry Overview