國立高雄大學圖資館 |

語系: 繁體中文

說明(常見問題)

圖資館首頁

登入

回首頁 到查詢結果 [ subject:"Pharmaceutical technology" ]

切換: 標籤 | MARC模式 | ISBD

Equipment qualification in the pharm...

Ostrove, Steven A.,

Equipment qualification in the pharmaceutical industry

紀錄類型:	書目-電子資源 : Monograph/item
正題名/作者:	Equipment qualification in the pharmaceutical industrySteven Ostrove.
作者:	Ostrove, Steven A.,
出版者:	London :Academic Press,2019.
面頁冊數:	1 online resource :col. ill.
標題:	Pharmaceutical technologyQuality control.
電子資源:	https://www.sciencedirect.com/science/book/9780128175682
ISBN:	9780128175699 (electronic bk.)

Equipment qualification in the pharmaceutical industry
Ostrove, Steven A.,

Equipment qualification in the pharmaceutical industry[electronic resource] /Steven Ostrove. - London :Academic Press,2019. - 1 online resource :col. ill. - Aspects of pharmaceutical manufacturing series. - Aspects of pharmaceutical manufacturing series..

Includes bibliographical references and index.

Front Cover; Equipment Qualification in The Pharmaceutical Industry; Copyright; Dedication; Contents; Acknowledgments; Introduction to aspects in pharmaceutical manufacturing; Chapter One: Introduction; Compliance; Qualification; Validate/validation; Types of qualification; The order of the qualification process; Chapter Two: Getting ready: Documentation; Overview; Documentation; Document specifics; Validation master plan; Drawings; Manuals; SOPs; Operations/vendors/others; Summary; Chapter Three: Quality systems; Quality risk management; Change control; Investigations

Equipment Qualification in the Pharmaceutical Industry provides guidance and basic information for the preparation of a quality qualification program. It has been noted that there is a general lack of understanding in the industry, especially for those new to the industry, as to what constitutes a compliant qualification program. Even experienced professionals have felt a lack of security in reaching a compliant state. This book outlines a guideline for the preparation and execution of qualification protocols including the installation (IQ), operational (OQ), and performance (PQ) protocols. It discusses the importance of related qualification programs (e.g., quality systems, commissioning, computer system, and cleaning) and how to incorporate them into a fully compliant qualification program. Furthermore, it provides matrices of what could be included in each type of protocol for major types of process equipment. While primarily for people entering the pharmaceutical industry, those established in the field will benefit from the multiple examples and matrices as well as integration of related systems. Equipment Qualification in the Pharmaceutical Industry provides students and pharmaceutical scientists a guideline for the preparation and execution of qualification (installation, operational, and performance) protocols.

ISBN: 9780128175699 (electronic bk.)Subjects--Topical Terms:

301575
Pharmaceutical technology
--Quality control.Index Terms--Genre/Form:

214472
Electronic books.

LC Class. No.: RS192

Dewey Class. No.: 615/.19

National Library of Medicine Call No.: 2019 G-986

Equipment qualification in the pharmaceutical industry
LDR:04507cmm a2200337 a 4500 001 601728
006 m o d
007 cr cnu|||unuuu
008 211110s2019 enka gob 001 0 eng d
020 $a 9780128175699 (electronic bk.)
020 $a 0128175699 (electronic bk.)
020 $a 9780128175682
020 $a 0128175680
035 $a (OCoLC)1104790565
035 $a on1104790565
040 $a N $b eng $c N $d N $d EBLCP $d OCLCF $d UKMGB $d OPELS $d UKAHL $d OCLCQ $d S2H $d OCLCO $d LVT $d UX1 $d VT2 $d OCLCA
041 0 $a eng
050 4 $a RS192
060 0 0 $a 2019 G-986
060 1 0 $a QV 736.1
082 0 4 $a 615/.19 $2 23
100 1 $a Ostrove, Steven A., $e author. $3 897208
245 1 0 $a Equipment qualification in the pharmaceutical industry $h [electronic resource] / $c Steven Ostrove.
260 $a London : $b Academic Press, $c 2019.
300 $a 1 online resource : $b col. ill.
490 1 $a Aspects of pharmaceutical manufacturing series
504 $a Includes bibliographical references and index.
505 0 $a Front Cover; Equipment Qualification in The Pharmaceutical Industry; Copyright; Dedication; Contents; Acknowledgments; Introduction to aspects in pharmaceutical manufacturing; Chapter One: Introduction; Compliance; Qualification; Validate/validation; Types of qualification; The order of the qualification process; Chapter Two: Getting ready: Documentation; Overview; Documentation; Document specifics; Validation master plan; Drawings; Manuals; SOPs; Operations/vendors/others; Summary; Chapter Three: Quality systems; Quality risk management; Change control; Investigations
505 8 $a Corrective action-Preventive actionCalibration/metrology; Preventive maintenance; Cleaning; Document control; Re-qualification; Chapter Four: Equipment design considerations; Materials of construction; Location; Cleaning and maintenance; Other considerations; Chapter Five: Equipment controls and automation; Structural qualification; Functional qualification; Black box, gray box, white box qualifications; IQ/OQ for computer or automated systems; Part 11; Summary; Chapter Six: Preparing the protocols: General approach; Protocol development; Layout; Stand-alone conditions; Acceptance criteria
505 8 $a Protocol reviewChapter Seven: Commissioning and decommissioning; FAT and SAT; Commissioning; Using commissioning data; Decommissioning; Chapter Eight: Equipment qualification protocols; Product contact; Criticality; Safety; System suitability; Environmental conditions; Protocols; Installation qualification; Operational qualification; Performance qualification; Protocol review; Chapter Nine: Equipment checklists; Chapter Ten: Protocol execution; Prioritization; Good documentation practices; Test instruments; Putting it all together; First steps; Second steps; Third steps
505 8 $a Handling deviations in the protocolPoints to remember; Summary of protocol execution; Chapter Eleven: Protocol reports; Preparing the report; Each section; Approval page; Purpose/scope; Conclusions; Results; Discussion; Deviations log; Appendix A: Definitions and abbreviations; Appendix B: Preparing a Qualification Protocol; Appendix C : References; Index; Back Cover
520 $a Equipment Qualification in the Pharmaceutical Industry provides guidance and basic information for the preparation of a quality qualification program. It has been noted that there is a general lack of understanding in the industry, especially for those new to the industry, as to what constitutes a compliant qualification program. Even experienced professionals have felt a lack of security in reaching a compliant state. This book outlines a guideline for the preparation and execution of qualification protocols including the installation (IQ), operational (OQ), and performance (PQ) protocols. It discusses the importance of related qualification programs (e.g., quality systems, commissioning, computer system, and cleaning) and how to incorporate them into a fully compliant qualification program. Furthermore, it provides matrices of what could be included in each type of protocol for major types of process equipment. While primarily for people entering the pharmaceutical industry, those established in the field will benefit from the multiple examples and matrices as well as integration of related systems. Equipment Qualification in the Pharmaceutical Industry provides students and pharmaceutical scientists a guideline for the preparation and execution of qualification (installation, operational, and performance) protocols.
650 0 $a Pharmaceutical technology $x Quality control. $3 301575
650 0 $a Pharmaceutical technology $x Standards. $3 520503
650 1 2 $a Drug Industry $x standards. $3 302855
650 2 2 $a Technology, Pharmaceutical $x standards. $3 520504
650 2 2 $a Equipment and Supplies $x standards. $3 190463
650 2 2 $a Quality Control. $3 225150
650 7 $a MEDICAL $x Pharmacology. $2 bisacsh $3 504870
655 0 $a Electronic books. $2 local. $3 214472
830 0 $a Aspects of pharmaceutical manufacturing series. $3 897209
856 4 0 $u https://www.sciencedirect.com/science/book/9780128175682