QMS Remediation in Pharma: :A Practical Guide to Restoring Compliance and Building Resilient Quality Systems
QMS Remediation in Pharma: A Practical Guide to Restoring Compliance and Building Resilient Quality Systems is a vital resource for QA professionals, regulatory experts, consultants, and executives tackling pharmaceutical QMS challenges. Written by Jonathon A. Rochelle, a QA leader with 25+ years of experience in Consent Decree remediations, this guide delivers a step-by-step roadmap to turn compliance failures into sustainable strengths.
Structured in five parts, it covers QMS basics and regulatory expectations, planning and gap assessments, core element remediation (e.g., CAPA, data integrity, supplier oversight), execution with project tools and metrics, and post-remediation culture building. Practical features include a stoplight KPI tracking guide, case studies, and appendices with templates like Remediation Master Plans, SOP checklists, and CAPA toolkits.
The book emphasizes risk-based strategies, cultural shifts, and continuous improvement. Ideal for responding to FDA 483s or EMA inspections, it equips readers to achieve robust compliance and resilient systems.
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QMS Remediation in Pharma: :A Practical Guide to Restoring Compliance and Building Resilient Quality Systems
QMS Remediation in Pharma: A Practical Guide to Restoring Compliance and Building Resilient Quality Systems is a vital resource for QA professionals, regulatory experts, consultants, and executives tackling pharmaceutical QMS challenges. Written by Jonathon A. Rochelle, a QA leader with 25+ years of experience in Consent Decree remediations, this guide delivers a step-by-step roadmap to turn compliance failures into sustainable strengths.
Structured in five parts, it covers QMS basics and regulatory expectations, planning and gap assessments, core element remediation (e.g., CAPA, data integrity, supplier oversight), execution with project tools and metrics, and post-remediation culture building. Practical features include a stoplight KPI tracking guide, case studies, and appendices with templates like Remediation Master Plans, SOP checklists, and CAPA toolkits.
The book emphasizes risk-based strategies, cultural shifts, and continuous improvement. Ideal for responding to FDA 483s or EMA inspections, it equips readers to achieve robust compliance and resilient systems.
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QMS Remediation in Pharma: :A Practical Guide to Restoring Compliance and Building Resilient Quality Systems

QMS Remediation in Pharma: :A Practical Guide to Restoring Compliance and Building Resilient Quality Systems

by Jonathon Rochelle
QMS Remediation in Pharma: :A Practical Guide to Restoring Compliance and Building Resilient Quality Systems

QMS Remediation in Pharma: :A Practical Guide to Restoring Compliance and Building Resilient Quality Systems

by Jonathon Rochelle

Paperback

$50.00 
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Overview

QMS Remediation in Pharma: A Practical Guide to Restoring Compliance and Building Resilient Quality Systems is a vital resource for QA professionals, regulatory experts, consultants, and executives tackling pharmaceutical QMS challenges. Written by Jonathon A. Rochelle, a QA leader with 25+ years of experience in Consent Decree remediations, this guide delivers a step-by-step roadmap to turn compliance failures into sustainable strengths.
Structured in five parts, it covers QMS basics and regulatory expectations, planning and gap assessments, core element remediation (e.g., CAPA, data integrity, supplier oversight), execution with project tools and metrics, and post-remediation culture building. Practical features include a stoplight KPI tracking guide, case studies, and appendices with templates like Remediation Master Plans, SOP checklists, and CAPA toolkits.
The book emphasizes risk-based strategies, cultural shifts, and continuous improvement. Ideal for responding to FDA 483s or EMA inspections, it equips readers to achieve robust compliance and resilient systems.

Product Details

ISBN-13: 9798319659323
Publisher: Barnes & Noble Press
Publication date: 08/26/2025
Pages: 446
Product dimensions: 8.50(w) x 11.00(h) x 0.90(d)

About the Author

Jonathon A. Rochelle is a seasoned quality assurance leader with over 25 years of experience in the pharmaceutical, biotechnology, blood banking, pharma and CLIA laboratories and dietary supplements industries, including more than 20 years in executive-level roles. Specializing in CAPA management, Lean transformations, manufacturing oversight, process improvement, and cultural transformation, he has successfully led multiple Consent Decree remediations, ensuring compliance with GMP, GLP, and GCP standards while fostering resilient quality systems. Jonathon has a proven track record of building and implementing robust QMS frameworks, including the design and rollout of electronic systems like TrackWise and Master Control across multi-site operations. His expertise extends to hosting regulatory audits, vendor qualification, and driving continuous improvement through metrics analysis and cross-functional collaboration.
Jonathon holds an AS degree from the Air Force in Medical Laboratory Technology, a BS in Microbiology from the University of Maryland University College, and a MS Certificate in Improving Global Health: Focusing on Quality and Safety from Harvard University's. He has also completed advanced coursework in Quality Assurance and Regulatory Affairs at Temple University. A passionate advocate for quality culture, Jonathon resides in Livingston, TX.
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