21 CFR 11, 210/211, 820, ICH Q7 - Good Manufacturing Practice Handbook
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GMP Boot Camp Training Certificate and GMP Handbook
13 November Training includes Registration Fee, and...
- 8 Hour Live GMP QMS & 21 CFR Part 11 Training Hosted by GMP Boot Camps and The Auditing Group. NOTE: The Training is Free, however, the cost is for the Certificate, E-Workbook and Handbook.
- Certificate of Attendance**
- Handbook, US FDA Title 21 CFR PARTS 11, 210/211 and 820 Pocket Guide.
- e-Workbook - Over 300+ Slides on a Note Style e-Workbook.
- Each person must register with a unique email address to get credit. for more information go to GMP Boot Camp website Terms.
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3 popular regulations in an easy to carry pocket handbook.
US FDA Title 21 CFR Part 11 Electronic Records; Electronic Signatures and includes Scope and Application 2003 - FDA Interpretation of Part 11 Requirements.
US FDA Title 21 CFR Parts 210/211 Good Manufacturing Practices - The regulations set forth in parts 210/211 contain the minimum current good manufacturing practice for methods to be used in, and the facilities or controls to be used for, the manufacture, processing, packing, or holding of a drug product.
US FDA Title 21 CFR Part 820 Quality Systems Regulation The methods used in, and the facilities and controls used for, the design, manufacture, packaging, labeling, storage, installation, and servicing of all finished devices intended for human use.
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**Must satisfy 7-hours on-line attendance to receive Certificate of Attendance
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- Guaranteed Lowest Price
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- Always Current, Up-To-Date
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- Special Customizations
- Pocket-sized 3.75" x 6.25"
- Prep for FDA & Client Audits
- Employee Training & Reference
- Promotional "giveaways"
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