21 CFR 11, 210/211, 820, ICH Q7 - Good Manufacturing Practice Handbook

GMP 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.
• - See www.gmpbootcamps.com for Free GMP QMS Training Schedule.

4 popular regulations in an easy to carry pocket handbook.

US FDA Title 21 CFR Part 11 Electronic Records; Electronic Signatures with Scope and Application 2003 - FDA Interpretation of Part 11.

US FDA Title 21 CFR Parts 210/211 Good Manufacturing Practices - The regulations containing the minimum CGMPs for methods, facilities or controls to be used for manufacture, processing, packing, or holding of a drug product.

US FDA Title 21 CFR Part 820 Quality Systems Regulation The controls used for, the design, manufacture, packaging, labeling, storage, installation, and servicing of all finished devices.

ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients.  The ICH Guidance supporting APIs for manufacturing of Drug Substance for Finished Products.

GMP Paper Certificate & E-Workbook

Paper Certificate** with Raised Seal great for mounting and displaying to verify your attendance to the GMP Boot Camp Training.

** Must satisfy 7-hours on-line attendance to receive
Certificate of Attendance!