Current Good Manufacturing Practice Training: A New Generation Series
In 8 one-hour segments, learn what the experts know about the CGMPs for Pharmaceutical and Biotech manufacturing.
If you are visiting here, ask yourself these three questions:
- Do you need to conduct CGMP Training on a limited budget?
- Do you want employees to learn the CGMPs from an expert using real examples?
- Do you 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.
 |
| Current Good Manufacturing Practice Training: A New Generation Series - GMP Online Training Courses |
Take action today!
- Learn more about our New Generation GMP online training series
- Call us: (415) 948-5220
Posts
