Regulatory: what is GxP?
Course
About course
This free, interactive course provides a high-level overview of GxP. This is an all-encompassing term that refers to various types of good practices for new drug development, such as good laboratory practice (GLP), good manufacturing practice (GMP), good clinical practice (GCP), and good documentation practice (GDP). This course will focus on GLP and GMP, with some reference to GCP and GDP.
Key learnings:
- Overview of the regulatory guidelines and what they entail
- How the guidelines fit in the regulatory process and how long they may take
- How the GxP requirements may differ between markets
After diving into the details, you’ll review a case study as well as find links to supporting resources. If you come across unfamiliar terms, check out the glossary of some key regulatory terms, processes, acronyms, and their definitions.
You can access and complete each lesson individually, with the full course taking around 20 minutes to complete.
Certification
You will get an online certificate after the course completion. You can view and download it in a section My Courses. With Cytiva Certificates, portions of our programs have been split into online modules, so you can earn a high quality knowledge in interactive format.
