Devine Guidance for Complying with the FDA’S Quality System Regulation: 21 CFR, Part 820

FDA Quality System Regulation for Medical Devices (21 CFR Part 820): A Practitioner's Guide to Management Controls (sections 820.20 Management ... 820.22 Quality Audit, and 820.25 Personnel)

Quality Risk Management in the FDA-Regulated Industry

Current Good Manufacturing Practices: Pharmaceutical, Biologics, and Medical Device Regulations and Guidance Documents Concise Reference

CAPA for the FDA-Regulated Industry

The FDA and Worldwide Quality System Requirements Guidebook for Medical Devices, Second Edition

Documentation Basics That Support Good Manufacturing Practices and Quality System Regulations

The Lean Six Sigma Pocket Toolbook: A Quick Reference Guide to 100 Tools for Improving Quality and Speed (Career (Exclude VGM))

ISO 13485: A Complete Guide to Quality Management in the Medical Device Industry

ISO 13485 Starter Guide