Cybersecurity for Pharma 4.0: Process Design and Quality Risk Management - Brossura

Joshi, Dr. Jayant; Naik, Umesh

Brossura

ISBN 13: 9798175015684

Casa editrice: Independently published, 2026

Riassunto

Cybersecurity for Pharma 4.0: Process Design and Quality Risk Management
Technology Alone Cannot Secure Your Supply Chain. If Your Processes Are Vulnerable, Your Enterprise is Defenseless.
In the era of Pharma 4.0, platforms like ERP, MES, LIMS, and IoT cold chain sensors deliver unprecedented speed and operational visibility. However, simply deploying advanced software without re-engineering the underlying workflows creates severe compliance, data integrity, and patient safety risks. A cybersecure digital supply chain is built through controlled, secure-by-design processes—not just firewalls and encryption.
In Cybersecurity for Pharma 4.0: Process Design and Quality Risk Management, industry experts Dr. Jayant Joshi and Umesh Naik provide the definitive blueprint for embedding cybersecurity directly into your daily operations, quality frameworks, and system validation lifecycles.
Inside Book 4 of this essential series, you will discover:

• Secure-by-Design Workflows: Learn to build cybersecurity directly into Digital SOPs, material traceability, batch release, exception handling, and recall readiness.
• Cyber-QRM Frameworks: Bridge the gap between IT security and pharmaceutical quality. Master proven tools like FMEA, HACCP-style mapping, and Bow-Tie analysis to evaluate cyber threats through a patient-safety lens.
• Computerized System Assurance (CSA): Shift from document-heavy validation to a risk-based CSA model. Confidently manage the full system lifecycle, from requirements (URS) and targeted testing (IQ/OQ/PQ, UAT, Regression) to secure system retirement.
• Critical Process Controls: Implement fail-safes such as segregation of duties, maker-checker approvals, and digital signatures to ensure every digital transaction is traceable and audit-ready.

Who This Book Is For:
Whether you are a Supply Chain Manager, Quality Assurance (QA) Director, Validation Engineer, IT/OT Process Owner, or Regulatory Affairs Specialist, this book equips you with the actionable frameworks to ensure your digital operations are fit for intended use.
Stop relying on technology to fix process vulnerabilities. Get your copy today and build a secure-by-design pharmaceutical enterprise!

Dettagli dell'edizione

• Editore: Independently published
• Data di pubblicazione: 2026
• Lingua: Inglese
• ISBN 13: 9798175015684
• Rilegatura: Tapa blanda
• Numero di pagine: 288
• Contatto del produttore: Printed by Amazon on behalf of the author; https://www.amazon.es/hz/contact-us; ; c/o Amazon Media EU S.à.r.l., 38 Avenue John F. Kennedy; Luxembourg; L-1855; Lussemburgo