Course Description
This six-hour course will highlight the main points for pharmaceutical good manufacturing practices defined in Title 21 of the Code of Federal Regulations, Part 210, Part 211, and Title 21 CFR Part 11 for Electronic Records, focusing on quality. Additionally, good documentation practices will be covered to ensure participants understand that documentation is essential for regulated industry compliance. The course has numerous opportunities for participants to discuss the application to their organization.
Course Specifics:
- Participant Cap - 30
- Delivery - Face-to-face or Virtual
- Course Length - Six (6) hours
- Printed Materials - Sent to company or college prior to delivery for them to print and disseminate