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26 produkter
21 CFR Part 11
Complete Guide to International Computer Validation Compliance for the Pharmaceutical Industry
E-bok, 2004
1131 kr
Lägg i varukorg
Covering regulatory requirements stipulated by the FDA, this book delineates the organization, planning, verification, and documentation activities and procedural controls required for compliance with worldwide computer systems validation regulations. The author introduces supporting technologies …
21 CFR Part 11
Complete Guide to International Computer Validation Compliance for the Pharmaceutical Industry
Häftad, 2019
1040 kr
Lägg i varukorg
Covering regulatory requirements stipulated by the FDA, this book delineates the organization, planning, verification, and documentation activities and procedural controls required for compliance with worldwide computer systems validation regulations. The author introduces supporting technologies …
Ensuring the Integrity of Electronic Health Records
The Best Practices for E-records Compliance
Häftad, 2020
846 kr
Lägg i varukorg
Data integrity is a critical aspect to the design, implementation, and usage of any system which stores, processes, or retrieves data. The overall intent of any data integrity technique is the same: ensure data is recorded exactly as intended and, upon later retrieval, ensure the data is the same …
Ensuring the Integrity of Electronic Health Records
The Best Practices for E-records Compliance
Inbunden, 2020
1566 kr
Lägg i varukorg
Data integrity is a critical aspect to the design, implementation, and usage of any system which stores, processes, or retrieves data. The overall intent of any data integrity technique is the same: ensure data is recorded exactly as intended and, upon later retrieval, ensure the data is the same …
21 CFR Part 11
Complete Guide to International Computer Validation Compliance for the Pharmaceutical Industry
Inbunden, 2004
3063 kr
Lägg i varukorg
Covering regulatory requirements stipulated by the FDA, this book delineates the organization, planning, verification, and documentation activities and procedural controls required for compliance with worldwide computer systems validation regulations. The author introduces supporting technologies …
Ensuring the Integrity of Electronic Health Records
The Best Practices for E-records Compliance
E-bok, 2020
999 kr
Lägg i varukorg
Data integrity is a critical aspect to the design, implementation, and usage of any system which stores, processes, or retrieves data. The overall intent of any data integrity technique is the same: ensure data is recorded exactly as intended and, upon later retrieval, ensure the data is the same …
Ensuring the Integrity of Electronic Health Records
The Best Practices for E-records Compliance
E-bok, 2020
999 kr
Lägg i varukorg
Data integrity is a critical aspect to the design, implementation, and usage of any system which stores, processes, or retrieves data. The overall intent of any data integrity technique is the same: ensure data is recorded exactly as intended and, upon later retrieval, ensure the data is the same …
Pharmaceutical and Medical Devices Manufacturing Computer Systems Validation
Häftad, 2021
562 kr
Lägg i varukorg
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 …
Data Integrity in Pharmaceutical and Medical Devices Regulation Operations
Best Practices Guide to Electronic Records Compliance
Häftad, 2022
562 kr
Lägg i varukorg
Data integrity is fundamental in a pharmaceutical and medical devices quality system. This book provides practical information to enable compliance with data integrity, while highlighting and efficiently integrating worldwide regulation into the subject. The ideas presented in this book are based …
EU Annex 11 Guide to Computer Validation Compliance for the Worldwide Health Agency GMP
E-bok, 2015
3744 kr
Lägg i varukorg
Good Manufacturing Practice (GMP) ensures medicinal products are produced consistently and controlled to the quality standards appropriate for their intended use and as required by product specifications or marketing authorization. Annex 11 details the European Medicines Agency (EMA) GMP …
21 CFR Part 11
Complete Guide to International Computer Validation Compliance for the Pharmaceutical Industry
E-bok, 2004
1266 kr
Lägg i varukorg
Covering regulatory requirements stipulated by the FDA, this book delineates the organization, planning, verification, and documentation activities and procedural controls required for compliance with worldwide computer systems validation regulations. The author introduces supporting technologies …
Pharmaceutical and Medical Devices Manufacturing Computer Systems Validation
Inbunden, 2018
2585 kr
Lägg i varukorg
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 …
Data Integrity in Pharmaceutical and Medical Devices Regulation Operations
Best Practices Guide to Electronic Records Compliance
E-bok, 2016
660 kr
Lägg i varukorg
Data integrity is fundamental in a pharmaceutical and medical devices quality system. This book provides practical information to enable compliance with data integrity, while highlighting and efficiently integrating worldwide regulation into the subject. The ideas presented in this book are based …
Pharmaceutical and Medical Devices Manufacturing Computer Systems Validation
E-bok, 2018
621 kr
Lägg i varukorg
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 …
Pharmaceutical and Medical Devices Manufacturing Computer Systems Validation
E-bok, 2018
641 kr
Lägg i varukorg
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 …
EU Annex 11 Guide to Computer Validation Compliance for the Worldwide Health Agency GMP
Inbunden, 2015
3480 kr
Lägg i varukorg
Good Manufacturing Practice (GMP) ensures medicinal products are produced consistently and controlled to the quality standards appropriate for their intended use and as required by product specifications or marketing authorization. Annex 11 details the European Medicines Agency (EMA) GMP …
EU Annex 11 Guide to Computer Validation Compliance for the Worldwide Health Agency GMP
E-bok, 2015
3744 kr
Lägg i varukorg
Good Manufacturing Practice (GMP) ensures medicinal products are produced consistently and controlled to the quality standards appropriate for their intended use and as required by product specifications or marketing authorization. Annex 11 details the European Medicines Agency (EMA) GMP …
Data Integrity in Pharmaceutical and Medical Devices Regulation Operations
Best Practices Guide to Electronic Records Compliance
Inbunden, 2016
2585 kr
Lägg i varukorg
Data integrity is fundamental in a pharmaceutical and medical devices quality system. This book provides practical information to enable compliance with data integrity, while highlighting and efficiently integrating worldwide regulation into the subject. The ideas presented in this book are based …
Data Integrity in Pharmaceutical and Medical Devices Regulation Operations
Best Practices Guide to Electronic Records Compliance
E-bok, 2016
660 kr
Lägg i varukorg
Data integrity is fundamental in a pharmaceutical and medical devices quality system. This book provides practical information to enable compliance with data integrity, while highlighting and efficiently integrating worldwide regulation into the subject. The ideas presented in this book are based …
Requirements of E-Records Integrity
E-bok, 2022
3777 kr
Lägg i varukorg
The worldwide medicines' manufacturing practices regulations depend heavily on reliable data and records. The information properly recorded is the basis for manufacturers to assure the regulatory authorities of product identity, strengths, purity, and safety. The collected electronic records …
Principios de Práctica Inmobiliaria en Florida
Av Orlando Lopez, Stephen Mettling m. fl.
Häftad, 2024
525 kr
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Principios de Práctica Inmobiliaria en Florida
Av Orlando Lopez, Stephen Mettling m. fl.
Häftad, 2026
499 kr
Lägg i varukorg
Implementation of a Data Reliability Program
Implementation of a Data Reliability Program
Häftad, 2025
458 kr
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Principios de Practica Inmobiliaria en Florida
Av Ryan Mettling, Stephen Mettling m. fl.
E-bok
328 kr
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