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GMP/ISO Quality Audit Manual for Healthcare Manufacturers and Their Suppliers

Book

GMP/ISO Quality Audit Manual for Healthcare Manufacturers and Their Suppliers

DOI link for GMP/ISO Quality Audit Manual for Healthcare Manufacturers and Their Suppliers

GMP/ISO Quality Audit Manual for Healthcare Manufacturers and Their Suppliers book

With Checklists and Software Package

GMP/ISO Quality Audit Manual for Healthcare Manufacturers and Their Suppliers

DOI link for GMP/ISO Quality Audit Manual for Healthcare Manufacturers and Their Suppliers

GMP/ISO Quality Audit Manual for Healthcare Manufacturers and Their Suppliers book

With Checklists and Software Package
ByLeonard Steinborn
Edition 6th Edition
First Published 2003
eBook Published 31 May 2019
Pub. Location Boca Raton
Imprint CRC Press
DOI https://doi.org/10.1201/9780429135941
Pages 448
eBook ISBN 9780429135941
Subjects Bioscience
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Steinborn, L. (2003). GMP/ISO Quality Audit Manual for Healthcare Manufacturers and Their Suppliers: With Checklists and Software Package (6th ed.). CRC Press. https://doi.org/10.1201/9780429135941

ABSTRACT

Volume 1 of this two-part package provides a complete set of checklists for internal and contract device and drug manufacturers and developers, contract software developers, and suppliers of chemical, printed material, electronic component, and general supplies. It also includes a simulated QSIT audit, and a new-product market launch. All of these

TABLE OF CONTENTS

part I|1 pages

Quality Audit Purpose and Practice

chapter 1|4 pages

Regulatory Considerations

chapter 2|5 pages

Quality Audits

chapter 3|7 pages

Internal Facility Audits

chapter 4|7 pages

Supplier Audits

chapter 5|3 pages

Contractor Audits

chapter 6|2 pages

Product Audits

chapter 7|5 pages

QSIT Audits

part II|1 pages

Quality Audit Checklists

chapter |41 pages

Internal Device Manufacturer/Developer Audit Checklist

chapter |49 pages

Contract Drug Manufacturer/Developer Audit Checklist

chapter |47 pages

Contract Device Manufacturer/Developer Audit Checklist

chapter |53 pages

Contract Drug Manufacturer/Developer Audit Checklist

chapter |29 pages

Contract Software Developer Audit Checklis

chapter |24 pages

General Supplier Audit Checklist

chapter |38 pages

Bulk Chemical Supplier Audit Checklist

chapter |26 pages

Printed Material Supplier Audit Checklist

chapter |25 pages

Electronic Component Supplier Audit Checklist

chapter |15 pages

QSIT Audit (New FDA Inspection Approach) for Medical Devices Checklist

chapter |13 pages

Qsit Audit (New Fda Inspection Approach) For Drug Company Checklist

chapter |19 pages

New Product Market Launch Checklist

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