Medical Device Quality Systems Manual

醫(yī)療器械質量體系手冊

A Small Entity Compliance Guide First Edition (Supersedes the Medical Device Good Manufacturing Practices [GMP] Manual)

小實體企業(yè)認證指南第一版(用于取代原醫(yī)療器械GMP手冊)

Chapters

章節(jié)

Cover page, Preface, Foreword

首頁，前言

Table of Contents

目錄

1. The Quality System Regulation

1. 質量體系法規(guī)

2. Quality Systems

2. 質量體系

3. Design Controls

3. 設計控制

4. Process Validation

4. 流程驗證

5. Personnel and Training

5. 人員和培訓

6. Buildings and Environment

6. 建筑和環(huán)境

7. Equipment and Calibration

7. 設備和校準

8. Device Master Record

8. 器械主記錄

9. Document and Change Control

9. 文檔和變更控制

10. Purchasing and Acceptance Activities

10. 采購和接收活動

11. Labeling

11. 標簽

12. Product Evaluation

12. 產品評價

13. Packaging

13. 包裝

14. Storage, Distribution and Installation

14. 存儲，分發(fā)和安裝

15. Complaints

15. 投訴

16. Servicing

16. 售后服務

17. Quality Systems Audits

17. 質量體系審計

18. Factory Inspections

18. 工廠檢查

19. Appendices

19. 附件

Cover page, Preface, Foreword

HHS Publication FDA 97-4179

首頁，前言

MEDICAL DEVICE QUALITY SYSTEMS MANUAL:

A SMALL ENTITY COMPLIANCE GUIDE

First Edition

(Supersedes the Medical Device Good Manufacturing Practices Manual)

Andrew Lowery, Judy Strojny, and Joseph Puleo

Division of Small Manufacturers Assistance

Office of Health and Industry Programs

CENTER FOR

DEVICES AND

RADIOLOGICAL HEALTH

CDRH

December 1996

(This publication supersedes FDA 91-4179)

U.S. DEPARTMENT OF HEALTH AND HUMAN SERVICES

Public Health Service

Food and Drug Administration

Center for Devices and Radiological Health

Rockville, Maryland 20850