Author: Mike Mulhearn

Veeva Vault Docs, Meet Agentic AI

The Problem: Agentic AI is only as useful as the context it can reach. When users ask an AI assistant a Vault-specific question — about VQL syntax, API endpoints, SDK behavior, object configuration, or platform features — the assistant needs access to accurate, current documentation. Without that, the workflow breaks down quickly: the user pauses…

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The Pharma IT Playbook Is Being Rewritten: What the Rise of Agentic AI Means for Life Sciences

Veeva’s 2026 R&D and Quality Summit in Copenhagen introduced three new AI product lines alongside roadmap updates across clinical, regulatory, safety, and quality. This post covers what each includes, where each stands on the release timeline, and what organizations with Veeva need to address before August. What “Agentic” Means Unlike conventional enterprise software, agentic AI…

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Practical Trial Master File (TMF) Lessons from ICH E6 (R3)

For nearly 30 years, the ICH GCP guideline has set the international standard of ethics and quality for conducting clinical trials.  The latest version, ICH GCP E6 (R3), was adopted on 06 Jan 25, an update 9 years in the making.  It contains an entire appendix dedicated to the Trial Master File.  Let’s explore some…

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