Pharma Foucs Europe
yokogawa-logo
yokogawa-data-integrity-pharma-manufacturing-live-webinar-banner yokogawa-data-integrity-pharma-manufacturing-live-webinar-sm-banner

Why Data Integrity Has Become a Boardroom Issue: How Tri-Integrity Enables Predictive Quality in Pharma Manufacturing

Learn how leading pharmaceutical manufacturers are connecting MES, LIMS, and eQMS through the Tri-Integrity approach to improve compliance, accelerate investigations, reduce quality risks, and build a Foundation for predictive quality.

10th November 2026 | 11:00 AM ET

What you will learn:

  • Understand why data integrity has become a boardroom issue for pharmaceutical manufacturers
  • Discover how Tri-Integrity connects MES, LIMS, and eQMS to strengthen compliance and quality performance.
  • Learn how predictive quality can reduce risk and support smarter GMP decision-making

Who should attend:

  • C-Level Executives
  • Business Management Leaders
  • VP / Head of Quality
  • QA/QC
  • Manufacturing
  • CSV
  • Business Management
  • Quality Assurance (QA)
  • Quality Management
  • Manufacturing Operations
  • Site Operations / Site Management
REGISTER NOW

Register Now

What systems has your organization already implemented?

What systems has your organization been currently evaluating?

May we contact you by email? *

Speakers:

Shahzad Khan-speaker

Shahzad Khan

Life Science Digital Solution Manager &
Global Solution Consultant –Yokogawa Corporation of America

  • Shahzad Khan expertise is in bioprocess automation, digital Transformation, and software solutions for the life sciences industry.
  • He works closely with pharmaceutical, biotechnology, and CDMO organizations to develop and implement innovative solutions that improve operational efficiency, data integrity, and manufacturing performance. He is actively involved in business development, strategic partnerships, and helping customers accelerate their digital transformation journey through automation and advanced software platform.