Why Should You Attend:
In this Webinar, the application of the terms GLP and GMP will be explored, as there is often confusion in their application during development. This presentation will define the terms and their application in the development environment.
During product development within an organization that has yet to commercialize a product, the use of the terms GLP and GMP are often confused and may be used incorrectly. Doing so can result in reducing credibility by regulatory health authorities, as well as cause confusion when working with collaborators. The objective of this seminar is to define the terms, what they mean and how they are applied.
Who Will Benefit:
This seminar would be beneficial to anyone that plays any leadership role in an FDA manufacturing environment to produce, test, warehouse and/or ship biologics or pharmaceuticals, including:
- Leaders in manufacturing
- Quality control
- Quality assurance
- Warehouse functions
- Directors/Managers in regulatory affairs
- Document control
- Development and nonclinical functions
For Registration: http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=701911?channel=eventsbot