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.
The GxP and Regulatory Series includes:
- 21 CFR Part 11
- Drug Safety: Adverse Event Reporting
- GCP1: Good Clinical Practice Level 1
- GCP2: Good Clinical Practice Level 2
- GLP: Good Laboratory Practice Overview
- GMP: Good Manufacturing Practice Overview
- GxP Industry Overview
Our e-courses are only available for group and corporate-wide licenses. Pricing is based on the estimated number of users. Please contact us to learn more about incorporating the GxP and Regulatory Series into your corporate training program. We can also develop custom training solutions to meet your specific training needs.