A consolidated list of articles, technical analysis, case studies, and reference material published by Nam Pham on pharmaceutical smart factory, ISA-95, MES/EBR, GxP validation, ALCOA+ data integrity, OT cybersecurity, and AI readiness for pharmaceutical manufacturing.
English articles on nampham.net
The English-language archive covers five clusters: ISA-95 and pharma automation (Cluster N1), GxP validation and compliance (Cluster N4), OT cybersecurity (Cluster N5), MES/EBR and paperless batch (Cluster N6), and industrial data and AI (Cluster N11). Each article links from the full list on /blog and is tagged with its cluster for cross-reference. Featured 2026 articles include the ISA-95 Implementation Roadmap, GxP Compliance and Validation Playbook, ALCOA+ Data Integrity guide, OT Cybersecurity per IEC 62443, MES/EBR Selection Guide, and AI/Data Science in Pharma Manufacturing.
Vietnamese articles on phamducphuongnam.com
The Vietnamese site (43 articles, /resources) covers the same topics in Vietnamese for the local market, with deeper technical detail and longer case write-ups. Categories include he-thong-san-xuat (production systems), gmp-compliance, mes-ebr, and audit-quality. The Vietnamese site is the primary SSoT for the Vietnamese-speaking market.
Whitepapers in progress
Reference Architecture for ISA-95 in Brownfield Pharmaceutical Sites, Data Integrity Assessment Checklist for Pharma Audits, OT/IT Interface Specification Template, MES Vendor Selection Decision Matrix, Computer Software Assurance (CSA) Implementation Playbook. Target completion Q3-Q4 2026.
Conference papers and proceedings
ISPE Asia Pacific Pharmaceutical Manufacturing Conference 2023, 2024. PDA Asia Pacific 2022, 2023. Vietnam Pharmaceutical Industry Association annual meetings 2021-2023. ISA Vietnam Section 2019, 2020. Topics included brownfield modernization, data integrity, OT/IT integration, and CSA implementation.
How to use this page
Use this Publications by Nam Pham page as a planning checkpoint before vendor selection, architecture review, validation scoping or implementation sequencing. The strongest next step is to compare the guidance with your current SOPs, system inventory, batch records, data flows and QA review routines so the discussion starts from evidence instead of assumptions.
Evidence to prepare
For Publications by Nam Pham, prepare the records, owners, risks and decision criteria linked to english articles on nampham.net, vietnamese articles on phamducphuongnam.com, whitepapers in progress, conference papers and proceedings. Useful evidence includes current process maps, interface lists, audit trail expectations, exception workflows, data retention rules and the business reason for changing the current operating model.
Frequently asked questions
Where can I find the full English article archive?
The full English archive is at /blog. The archive includes 25 published articles across five clusters (N1, N4, N5, N6, N11) covering ISA-95, GxP validation, OT cybersecurity, MES/EBR, and industrial data/AI.
Is there a Vietnamese version of the articles?
Yes. The Vietnamese site at phamducphuongnam.com has 43 articles covering the same topics in Vietnamese for the local market. The Vietnamese site is the primary SSoT for the Vietnamese-speaking market.
Contact via /contact with the topic, target audience, and the question the article should answer. The editorial calendar prioritizes topics that help a pharmaceutical engineering team act on a real decision within 30 days.