Data Integrity in Pharmaceutical and Medical Devices Regulation Operations : Best Practices Guide to Electronic Records Compliance
Data Integrity in Pharmaceutical and Medical Devices Regulation Operations : Best Practices Guide to Electronic Records Compliance
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Author(s): Lopez, Orlando
ISBN No.: 9781498773249
Pages: 372
Year: 201610
Format: Trade Cloth (Hard Cover)
Price: $ 213.93
Dispatch delay: Dispatched between 7 to 15 days
Status: Available (On Demand)

Orlando Lopez 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. ons.


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.


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