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Overcome Roadblocks, Identify Solutions and Implement Processes for a Successful Data Governance Program

August 15-16, 2018
  • Cambridge, MA

With FDA and MHRA attention pinpointed on data integrity issues in recent 483s and warning letters, it is critical to prepare your validation and quality departments with the tools and resources to ensure data integrity in manufacturing processes. IVT’s 4th Annual Data Integrity Validation provides a wide range of industry perspectives in an unmatched training environment, diving deep into the nuances of building and maintaining a compliant data governance program across company-wide systems.


  • It’s Elementary!
    Detecting Data Integrity Lapses in the Innovations in the Cloud
    — Simplifying the Quality Systems Validation Process
  • Navigate Data Integrity Expectations in the GCP Environment
  • How Not to Crash and Burn During Your Next
    Agency Inspection
  • Interpret FDA and MHRA Guidelines From a
    Manufacturing Mindset
  • “Homo Sapiens atque Integritas Notitia”
    (Human Beings and Data Integrity)
    Ask the Experts — Open Audience Q&A to Discuss
    Core Data Integrity Concepts and Challenges


Choose from Two Customized Hands-On Workshops:

Implement a Data Governance Plan that Suits Your Organization’s Processes

Utilize the GAMP Data Integrity Maturity Model to Assess Your Effectiveness

Previous Attendee Acclaim:

If you need ideas to mitigate data integrity issues,
you have to join this conference.

Head, GYPIT Audit Management, Bayer Pharma

Very nice discussions and presenters that help us to
have an industry perspective on new trends.

QA Specialist, Corp. GxPCRs, Amgen

Best way to learn and share industry thoughts.

Director/Head of QA, CSV, Gilead

A lot of useful information was presented. This will be
very helpful in fulfilling my job responsibilities.


Very good information. IVT does an excellent job at bringing
a diverse array of talent to these conferences.

Senior Manager, Systems and Technology, Celgene

Tangible knowledge to bring back to work and implement.

CSV Specialist, Par Sterile Products

First time to conference. Great insight into what needs to
be done and what steps need to be taken.

Manager QC Lab, Young Living Essential Oils