GMP Publications - Code of Federal Regulation Handbooks by the FDA

GLP Master Handbook

GLP-Master4.5x7.jpg
978-1-935131-09-0

US FDA Title 21 CFR Parts

Part 11 - Electronic Records
Part 58 - Good Laboratory Practice
Part 210/211 - cGMP in Manufacturing, Processing, Packaging or Holding of Drugs and Finished Pharmaceuticals
Part 606 - GMP for Blood and Blood Components
Part 610 - General Biological Products Standards
Part 820 - Quality Systems Regulations

US Health and Human Services Public Health

Title 42 CFR Part 493 Laboratory Requirements

OECD - Organisation for Economic Co-Operation And Development

General Principles of GLP Series 1











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