A consolidated record of conference talks, panel discussions, webinars, podcasts, and industry presentations delivered by Nam Pham on pharmaceutical engineering, GxP validation, OT cybersecurity, ISA-95 integration, and AI readiness.
ISPE Asia Pacific Conference 2026 — Brownfield ISA-95 Modernization: A 5-Year Roadmap for Vietnamese Pharma Manufacturers. Webinar Q3 2026 — ALCOA+ Data Integrity in Practice: 10 Common Audit Findings.
ISPE Vietnam — GxP Validation for AI/ML Systems. PDA Asia Pacific — Annex 11 Implementation: 5 Years Later (panel). VPIA annual — Smart Factory in Practice: Lessons from 10 Pharma Sites in Vietnam.
ISPE Asia Pacific (Singapore) — OT/IT Integration Without Breaking Compliance. ISA Vietnam — PLC/HMI Modernization in GMP Environments. Vietnam Pharma Summit — Computer Software Assurance for Vietnamese Manufacturers.
ISPE Asia Pacific — Data Integrity in Practice. PDA Asia Pacific — Annex 11 roundtable moderator. MOH Vietnam GMP Inspector Training (observer). ESEC internal tech talk series (monthly). ISA Vietnam — OPC-UA in Pharma. ISPE Vietnam Local Chapter founding contributor.
Use this Talks and Speaking Engagements 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.
For Talks and Speaking Engagements, prepare the records, owners, risks and decision criteria linked to 2026 (planned), 2025, 2024, 2023 and earlier. 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.
Brownfield ISA-95 modernization, GxP validation for AI/ML, ALCOA+ data integrity, OT cybersecurity per IEC 62443, MES/EBR vendor selection, AVEVA PI System, and Computer Software Assurance (CSA) implementation.
Contact via /contact with event name/date/location, audience profile, topic or question the talk should address, honorarium policy, and recording policy. Lead time: 6-8 weeks for new material, 2-3 weeks for repeat topics.
In-person events: negotiated case by case. Webinars: usually recorded with speaker approval. Internal corporate talks: not recorded, materials returned or destroyed per client policy.