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Good Design Practices for GMP Pharmaceutical Facilities 2nd Edition by Terry Jacobs, Andrew Signore ISBN 1315355027 9781315355023

Name: Good Design Practices for GMP Pharmaceutical Facilities 2nd Edition by Terry Jacobs, Andrew Signore ISBN 1315355027 9781315355023
SKU: EB-5507136
Availability: InStock

Original price was: $50.00.Current price is: $25.00.

Good Design Practices for GMP Pharmaceutical Facilities Second Edition Terry Jacobs Digital Instant Download

Author(s): Terry Jacobs, Andrew A. Signore

ISBN(s): 9781482258905, 1482258900

Edition: 2

File Details: PDF, 21.10 MB

Year: 2016

Language: English

SKU: EB-5507136 Category: Business & Economics - Industries Tags: Andrew A. Signore, Terry Jacobs

Description

Good Design Practices for GMP Pharmaceutical Facilities 2nd Edition by Terry Jacobs, Andrew A. Signore – Ebook PDF Instant Download/Delivery: 1315355027, 978-1315355023
Full download Good Design Practices for GMP Pharmaceutical Facilities 2nd Edition after payment

Product details:

ISBN 10: 1315355027
ISBN 13: 978-1315355023
Author: Terry Jacobs, Andrew A. Signore

This revised publication serves as a handy and current reference for professionals engaged in planning, designing, building, validating and maintaining modern cGMP pharmaceutical manufacturing facilities in the U.S. and internationally. The new edition expands on facility planning, with a focus on the ever-growing need to modify existing legacy facilities, and on current trends in pharmaceutical manufacturing which include strategies for sustainability and LEED building ratings. All chapters have been re-examined with a fresh outlook on current good design practices.

Good Design Practices for GMP Pharmaceutical Facilities 2nd Table of contents:

Chapter 1 Pharmaceutical Industry Profile

Chapter 2 Current Good Manufacturing Practices

Chapter 3 Legacy Facility Master Planning

Chapter 4 Architectural Design Issues

Chapter 5 Facility Utility Systems

Chapter 6 High-Purity Water

Chapter 7 Commissioning, Qualification, and Validation

Chapter 8 Process Engineering

Chapter 9 Oral Solid Dosage Facilities

Chapter 10 Continuous Oral Solid Dose Processing

Chapter 11 Sterile Manufacturing Facilities

Chapter 12 Biotechnology Facilities

Chapter 13 Codes and Standards

Chapter 14 Containment Technology

Chapter 15 Occupational Health and Safety

Chapter 16 Sustainability

Chapter 17 QA/QC Laboratories and Related Support Spaces

Chapter 18 Packaging and Warehousing

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