Single-Use Technology : : A Practical Guide to Design and Implementation / / Adriana G. Lopes, Andrew Brown.

Single-Use Technology (SUT) is the first comprehensive publication of practical considerations for each stage of the implementation process of SUT, and covers the selection, specification, design and qualification of systems to meet end-user requirements. Having become readily available for all proc...

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Superior document:Title is part of eBook package: De Gruyter DG Plus eBook-Package 2019
VerfasserIn:
Place / Publishing House:Berlin ;, Boston : : De Gruyter, , [2019]
©2019
Year of Publication:2019
Edition:2nd edition
Language:English
Series:De Gruyter STEM
Online Access:
Physical Description:1 online resource (VIII, 146 p.)
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100 1 |a Lopes, Adriana G.,   |e author.  |4 aut  |4 http://id.loc.gov/vocabulary/relators/aut 
245 1 0 |a Single-Use Technology :  |b A Practical Guide to Design and Implementation /  |c Adriana G. Lopes, Andrew Brown. 
250 |a 2nd edition 
264 1 |a Berlin ;  |a Boston :   |b De Gruyter,   |c [2019] 
264 4 |c ©2019 
300 |a 1 online resource (VIII, 146 p.) 
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505 0 0 |t Frontmatter --   |t Preface --   |t Contents --   |t 1. Introduction --   |t 2. Strategies for implementation of single-use technology: A risk- and science-based approach --   |t 3. Feasibility assessment of single-use technology and suppliers --   |t 4. Specifications and design of single-use technology --   |t 5. Validation --   |t 6. Case studies --   |t Abbreviations --   |t Appendix 1 Scoring Tables --   |t Appendix 2 Risk Rating and Priority Number --   |t Index 
506 0 |a restricted access  |u http://purl.org/coar/access_right/c_16ec  |f online access with authorization  |2 star 
520 |a Single-Use Technology (SUT) is the first comprehensive publication of practical considerations for each stage of the implementation process of SUT, and covers the selection, specification, design and qualification of systems to meet end-user requirements. Having become readily available for all processing operations within the biopharmaceutical industry, SUT has the potential to reduce capital costs, improve plant throughput and reduce the risk of cross-contamination. However, there are no clear guidelines to aid the end-user on implementation of these technologies into a validated, good manufacturing practice (GMP) environment. This book presents approaches for the implementation within various end-user facilities and systems, SUT within regulatory frameworks (ICH Q8, Q9, Q10 and GMP), standardisation and assessment strategies, specifation of user requirements and SUT design, risk assessment and evaluation as well as qualification for different SUT types. 
538 |a Mode of access: Internet via World Wide Web. 
546 |a In English. 
588 0 |a Description based on online resource; title from PDF title page (publisher's Web site, viewed 30. Aug 2021) 
650 0 |a Medical supplies, Disposable. 
650 0 |a Pharmaceutical biotechnology. 
650 4 |a Biopharmazeutikum. 
650 7 |a SCIENCE / Chemistry / Industrial & Technical.  |2 bisacsh 
653 |a Biopharmaceutical. 
700 1 |a Brown, Andrew,   |e author.  |4 aut  |4 http://id.loc.gov/vocabulary/relators/aut 
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