The FDA's Good Laboratory Practices (GLP) regulations are what ultimately determine whether your product will advance to the clinical stage, and thus, to market. Understanding how GLP impacts your products and business is crucial to developing successful products.
If you and your colleagues are interested in learning how to use GLPs to make a significant impact on your organization's research and compliance efforts, then join us for this interactive 90-minute webinar:
This interactive, 90-minute session will give you a foundational understanding of GLP, why it is important, and how to comply. By attending this session, you will learn:
- The bedrock principles that form GLP, why they are critical, and how to follow them
- The ability to establish a GLP-compliant culture within your department or organization
- How to recognize GLP deficiencies through the use of case studies and recent examples of official FDA findings
- The regulations themselves – what you need to know
By the end of this session, you will feel confident enough in your knowledge of GLP to make a significant impact on your organization's research and compliance efforts.