Orlando Lopez

EU Annex 11 Guide to Computer Validation Compliance for the Worldwide Health Agency GMP (eBook, ePUB)

• Format: ePub

Produktbeschreibung

This book provides practical information to enable compliance with computer systems requirements, while highlighting and integrating the Annex 11 guidelines into the computer compliance program. The ideas presented in this book are based on the author's twenty five years of experience with computer validation in the healthcare industry with various computer systems development, maintenance, and quality functions. A practical approach is presented to increase efficiency and to ensure that software development and maintenance is achieved correctly.

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Produktdetails

• Verlag: Taylor & Francis
• Erscheinungstermin: 6. April 2015
• Englisch
• ISBN-13: 9781040083703
• Artikelnr.: 72269352

Autorenporträt

Orlando L¿pez

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.

Inhaltsangabe

Introduction. SLC, Computer Validation, and Annex 11. Annex 11 Principles.
Risk Management. Personnel. Suppliers and Service Providers. Validation.
Data. Accuracy Checks. Data Storage. Printouts. Audit Trails-Ensuring Data
Integrity. Change and Configuration Management. Periodic Evaluation:
Independent Review to Ensure Continued Validation of Computerized Systems.
Security. Incident Management. Electronic Signatures: Electronic Signing
Requirements. Batch Certification and Release. Business Continuity.
Archiving. SLC Documentation. Relevant Procedural Controls. Maintaining the
Validated State in Computer Systems. Annex 11 and the Cloud. EU GMP Chapter
4-Documentation and Annex 11. Annex 11 and Electronic Records Integrity.
Annex 11 and 21 CFR Part 11: Comparisons for International Compliance.