Enterprise AI has moved beyond experiments. In 2026, success isn’t about adding an LLM - it’s about building agentic systems that scale, govern themselves, and deliver ROI in production . While 79% of enterprises have adopted AI agents , only 23% have scaled them across the organization . The gap isn’t intent - it’s architecture. The Market Reality AI agent market: $7.3B (2025)  → $199B by 2034 88% of enterprises  use AI regularly 74% of leaders  see ROI within the first year

For many life sciences organizations, a Veeva Vault go-live marks a milestone moment. Months of workshops, validation cycles, migration effort, and user training finally converge. Teams celebrate. Leadership feels confident. Users explore with optimism. And then…the cracks slowly appear. Performance frustrations. Process inefficiencies. Endless enhancement requests. Frustrated users. Concerns that “Vault isn’t delivering the value we expected.” In most cases, Vault doesn’t fa

How 900 Million People Use Artificial Intelligence Every Day—And Most  Don't Even Know It   Analysis | December 2025   Here's a peculiar fact about the future: it sneaks up on you while you're busy  checking the weather.    Right now, as you read this, approximately 900 million people worldwide are  actively using artificial intelligence tools. That's roughly 11% of humanity. But  here's the twist that makes this statistic genuinely interesting: according to a Gallup  survey 

Introduction Document migration is often treated as a prerequisite activity in Veeva Vault programs, something that needs to be completed before real value can be realised. In regulated environments, however, migration is far more than a technical step. It directly influences data integrity, inspection readiness, and long-term trust in the platform. Over multiple Vault programs, we’ve seen that migration challenges rarely stem from tooling limitations. They arise from underes

The Evolution: How Software Development Reached the “Vibe Coding” Era Not long ago, building software followed a painfully familiar path: long planning cycles, detailed specifications, months of development - and only then, real user feedback. By the time products reached users, market needs had often already shifted. That rhythm began to break in late 2024 and accelerated through 2025 , when AI-powered development assistants became mainstream. Around this time, Andrej Karpat

Veeva Vault 25R3 delivers a focused and meaningful set of enhancements for Regulatory Affairs, Submissions, RIM, Archive, and Safety (PV) teams. The updates aren’t flashy — they’re operational, compliance-driven, and designed to improve quality, reduce rework, and strengthen global inspection readiness. Across Regulatory & Safety, the release centers on four themes Higher-quality submission packages with stronger validation Improved handling of secure & signed content Stronge

Veeva’s 25R3 release strengthens Commercial Content Operations and Medical Review by reducing cycle time, improving compliance, and elevating content quality before MLR. The highlight is the introduction of AI-driven automation — especially the Quick Check Agent and the AI Chat Assistant.   Below is a structured, operations-ready breakdown of the seven most impactful features, written in the requested format and paired with Wolvio’s Insight. 1. AI Quick Check Agent Applies to

The Hold Music Era Is Finally Over A Data-Driven Deep Dive into the $47.5 Billion Voice Revolution Why Are We Suddenly Talking About Voice Agents? Let's cut through the noise. Three things happened simultaneously that turned voice AI from a "someday" technology into a "right now" business imperative: 1. Latency cracked the 800ms barrier. Human conversational response time sits around 300-500 milliseconds. Old AI systems took 2-5 seconds—an eternity that screams "robot." Today

Veeva Vault 25R3 may not be flashy, but it delivers powerful, practical updates that are critical for GxP environments. If you work in Quality Management, QualityDocs, or change control, this release focuses on closing compliance gaps, improving efficiency, and strengthening external collaboration. This release focuses on practical improvements: more reliable controlled copy reconciliation, smarter management of change control, and enhanced flexibility for quality actions inv

Veeva Vault 25R3 updates aren’t a dramatic release, but they’re an important one. The Veeva Clinical Operations 25R3  release includes several significant updates for clinical teams. If you work in clinical operations, CTMS, SSU, or eTMF, you’ll notice the difference almost immediately. These updates don’t aim to impress—they aim to fix long-standing gaps, strengthen accuracy, and make everyday work smoother. This release focuses on practical improvements: more accurate metr

Veeva Vault 25R3 introduces a powerful set of features designed to elevate user experience and operational efficiency. From smarter data validation with Duplicate Detection to seamless session management through the Multi-Vault Experience, this release focuses on visibility, automation, and control. Discover how innovations like Process Monitor, Asynchronous Workflows, and Secure PDF Control streamline workflows and empower teams to work smarter across the platform.

The introduction of Agentic AI within Veeva Vault represents a monumental shift for regulated industries, revolutionizing how data is handled, compliance is ensured, and productivity is driven through intelligence embedded in every workflow. At Wolvio Solutions, we closely monitor this evolution, aligning our consulting capabilities with Veeva’s roadmap to prepare clients and partners for the future of life sciences platforms. The Veeva AI Journey: Milestones and Industry Imp

Every Veeva Vault release is more than an update — it’s a step forward in smarter, compliant digital operations. The 25R3 release, coming this December, brings platform enhancements, improved usability, and deeper integration across Vault applications. Learn how early impact assessment, alignment, and proactive testing can turn 25R3 readiness into a strategic advantage for both business and IT teams.

In the life sciences industry, regulatory compliance is not just a requirement, it is the foundation of trust between companies,...

Executive Summary The implementation of a digital promotional content management solution such as Veeva Vault PromoMats 1.0 represents a...

MedComms approved it. ✅ But PromoMats said ❌. What should’ve been a seamless transfer turned into a compliance mess — delays, re-approvals, and endless frustration. At Wolvio Solutions, we tackled this head-on with a custom SDK Vault-to-Vault integration that brought automation, clarity, and compliance back to the table. Read how we turned “Why is this so hard?” into “Finally, it works.”

So You’re Loading Documents into Veeva Vault… Now What? You’re just one week away from your big go-live. Thousands of documents are piled...

Unlock the power of Veeva Vault Clinical’s Milestones & EDLs object model with our clear visual explainer. Learn how template-driven milestones align with expected documents across Study, Country, and Site levels—driving automation, inspection readiness, and CTMS/eTMF success. This infographic breaks down parent-child relationships, EDL factoring, and triggers for smarter clinical trial management.

Release Impact Assessment Series: Key Clinical Features in Veeva Vault 25R1!

🚀 Veeva Vault 25R1 is here! Our Release Impact Assessment (RIA) Series highlights 8 key platform features