Deliberate Documentation
Deliberate Documentation is an overview of the documentation requirements of Good Manufacturing Practice (GMP) and stresses the importance and benefits of a disciplined approach to documentation in an FDA (Food and Drug Administration) regulated environment. Prior enrollment in GMP Orientation/Refresher or experience in an FDA regulated industry is recommended.
Primary Audience: Industry
Secondary Audience:
Primary Industry Sector:
Secondary Industry Sector: na
Program Type: Continuing Education
Lecture Hours: 3
Lab Hours:
For more information about Deliberate Documentation in your area, please select your region below:
| Western NC | |
| Charlotte Region | |
| Eastern NC | |
| Southeastern NC | |
| Northeastern NC | |
| Piedmont Triad | |
| Research Triangle |