Pharmaceutical and Medical Devices Manufacturing Computer Systems Validation
Language: English
Published by CRC Press, 2021
- Softcover
- Used
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: Este libro proporciona información práctica para ayudar en la validación de sistemas informáticos para sistemas de producción, destacando e integrando eficientemente la regulación mundial en el tema. Se presenta un enfoque práctico para aumentar la eficiencia y garantizar que la validación de los sistemas informáticos se logre correctamente. Es relevante para las operaciones reguladas de dispositivos farmacéuticos y médicos. EAN: 9781032094700 Tipo: Libros Categoría: Tecnología|Salud y Bienestar|Ciencias|Negocios y Economía Título: Pharmaceutical and Medical Devices Manufacturing Computer Systems Validation Autor: Orlando Lopez Editorial: CRC Press Idioma: en Páginas: 344 Formato: tapa blanda.
Seller Inventory # Happ-2024-03-15-b5bec028
- Title
- Pharmaceutical and Medical Devices Manufacturing Computer Systems Validation
- Author
- Orlando Lopez
- Publisher
- CRC Press
- Publication year
- 2021
- Condition
- Very Good
- Binding
- Soft cover
- Language
- English
- ISBN 10
- 1032094702
- ISBN 13
- 9781032094700
Validation of computer systems is the process that assures the formal assessment and report of quality and performance measures for all the life-cycle stages of software and system development, its implementation, qualification and acceptance, operation, modification, requalification, maintenance and retirement (PICS CSV PI 011-3). It is a process that demonstrates the compliance of computer systems functional and non-functional requirements, data integrity, regulated company procedures and safety requirements, industry standards, and applicable regulatory authority’s requirements. Compliance is a state of being in adherence to application-related standards or conventions or regulations in laws and similar prescriptions.
This book, which is relevant to the pharmaceutical and medical devices regulated operations, provides practical information to assist in the computer validation to production systems, while highlighting and efficiently integrating worldwide regulation into the subject. A practical approach is presented to increase efficiency and to ensure that the validation of computer systems is correctly achieved.
"Synopsis" may belong to another edition of this title.
About the Author
Orlando López
E-records Integrity SME
Durham North Carolina USA
Orlando Lopez has significant understanding and experience with worldwide regulatory authorities regarding CSV, e-records integrity, and related requirements/guidelines related to Production Manufacturing Systems, IT Systems, Analytics, and Business Intelligence.
He has knowledge and experience in the development of governance and SLC deliverables. Wrote and deployed CSV methodology to computer infrastructure J&J worldwide. Several times he had re-engineered the computer validation methodology to regulated companies.
Orlando Lopez has experience with direct participation in FDA agency remedial action plans, regulatory inspections, response activities, and consent decree remediation related verifications.
He is published in the Encyclopedia of Pharmaceutical Science and Technology, 4th Edition - Chapter 56 Computer Systems Validation (Taylor & Francis Group, LLC) and had written 25+ publications, including 9 computer compliance related books - amazon.com/author/orlandolopez/
Familiar with gap assessment, remediation planning and remediation execution activities.
"About the title" may belong to another edition of this title.
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