I speak on validating AI in GxP and on the move from CSV to CSA

I've spoken at 70+ global forums and delivered 75+ international webinars. The talks come from the work I do with quality teams every week, validating real systems and deciding how much evidence is enough.

Meet me at KENX in Amsterdam on 14 and 15 October 2026. If you'll be there, book a time to talk and we'll find a slot between sessions.

Coming up

Where I'm speaking next

14 and 15 October 2026 · Amsterdam

KENX AI in GxP Europe

I'm a confirmed speaker at the Four Elements hotel in Amsterdam. My conference session is “How AI Is Transforming Deviations and the Evolving Role of Quality”, and I also lead 2 lunch and learn sessions over the 2 days. KENX publishes the times on its agenda.

15 October 2026 · Online

Scilife Quality Summit 2026

I'm a confirmed speaker. I share the opening session with Martin King: he covers AI governance and regulation, and I pick up with how to validate AI in GxP. A joint discussion and audience questions follow.

Past talks

Talks I've given

6th Annual Computer Software Assurance conference, Eminence Business Media, live online, September 2026. 2 sessions: the hybrid record trap on 3 September, and assessing AI readiness under FDA CSA on 4 September.
Scilife webinar, June 2026. The CSV to CSA roadmap for modernising GxP validation.
Compliance Associates webinar, May 2025. Digital automation of the APQR.
ICSVC congress, Brussels, October 2024. Quality management systems and automation in pharma.
KENX LEAN Validation, Philadelphia, June 2024.
CSV DMSO Conference, April 2024.
KENX Validation University, Philadelphia, March 2023.

These are the recent ones. The full count is 70+ global forums and 75+ international webinars. You'll find my articles and papers on the Publications page, and the organisations I work with on the Customers page.

Topics

What I speak about

AI validation in GxP

How to validate an AI system that learns and drifts, and what an inspector will ask you about it.

CSV to CSA

How to move a team from heavy documentation to risk-based testing, with evidence an inspector will accept.

EU GMP Annex 22

What the draft AI annex asks of a regulated company, from someone who contributed to the industry review.

Paperless validation

What I learned taking validation off paper across 40+ sites, and the mistakes worth avoiding.

How to invite me

Send me the event, the audience, the date and the topic you have in mind, and I'll reply myself. Write to info@trustbridge-compliance.com or book a short call.

Talk to Sachin Email me