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

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.

Learn how to efficiently update the TMF Index in Vault Clinical with this quick and easy guide. Streamline your process, ensure compliance,

What is the eCTD Compliance Package? An eCTD Compliance Package for promotional materials is a structured submission prepared in the...

One of Vault's standout features is Soft Deletion, which offers flexibility in handling content without sacrificing traceability.

Introduction: In the evolving landscape of clinical data management, pharma companies are continually seeking more efficient ways to...

Introduction Clinical trials are the backbone of medical progress, bringing new drugs and therapies to patients. However, managing these...

As a life sciences company using Veeva Vault, ensuring the security and compliance of your data is crucial. With the increasing reliance...

Veeva RegulatoryOne is part of Veeva Systems’ suite of cloud-based applications tailored for regulated industries.

Elevating Quality Control Across Industries with Veeva Vault QualityOne

Introduction Regulatory submission is a critical process in industries such as pharmaceuticals, biotechnology, medical devices, and other...

Introduction : In a previous blog post, We have unveiled TMF Management: Harnessing the Power of AI with Veeva Vault TMF Bot ...

Introduction : Artificial Intelligence (AI) is reshaping the landscape of clinical research and pharmaceuticals, particularly through...

Introduction "Custom security configurations in Veeva Vault empower organizations to answer the fundamental question of 'who can access...

Introduction In the realm of clinical trials and regulatory submissions, the management of Trial Master File (TMF) indexes is not just...

Introduction Effectively managing suppliers is an ongoing challenge for organizations striving for operational excellence. Qualifying...

Introduction In the domain of clinical operations concerning the management of clinical trial data and documents, the transition from...

Problem Statement: Using legacy CTMS technology that was not adaptive to today’s clinical trials, lack real time visibility and was...

Problem Statement: ‌Organizations often struggle with effectively managing and tracking their quality processes and documentation,...

Problem Statement: ‌‌ Maintaining a separate Digital Asset Management system can be expensive, complex, difficult to main and a risk of...