Current Good Manufacturing Practice Training
A New Generation Series
- In 8 one-hour CGMP training segments, learn what the experts know about the CGMPs for Pharmaceutical and Biotech manufacturing
- Learn more, view the details for CGMP Online Training: A New Generation Series
Ask yourself these three questions about CGMP training:
Do you . . .
- need to conduct CGMP Training on a limited budget?
- want employees to learn the CGMPs from an expert using real examples?
- need CGMP Training resources suitable for multiple levels of the organization?
If you answered YES to any of these three questions then you should take a look at the courses below:
- 21CFR211 – Learn the highlights of the Current Good Manufacturing Practice Regulations.
- Your Personal Responsibilities – Part B. Review the requirements for personnel working in the pharmaceutical industry.
- Foundation to Facility – Part C. Dive into the requirements for the design, cleaning & maintenance of a facility.
- Maintaining Compliant Equipment Practices – Part D. Examine the requirements for the design, cleaning & maintenance of equipment.
- Supplier to Plant – Part E. Explore the requirements for the receipt, storage and use of all components.
- Plan to Production – Part F. Review the requirements for production process controls and validation.
- Plant to Patient – Part G, H, & K. Examine the requirements for packaging, labeling, warehousing and distribution.
- Laboratory to Release – Part I. Dive into the requirements for laboratory controls, method validation, stability and more!
- Proper Documentation Practices – Part J. Examine the requirements for proper paper and electronic documentation practices.