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What is Veeva Vault QMS?

Elevate quality standards and ensure adherence to GxP regulations through Vault QMS, which integrates proven best practices and automated workflows to unify all participants, including pharmaceutical and biotech companies, contract manufacturers, and suppliers, into a streamlined quality management system for enhanced oversight and control. This innovative system fosters effortless collaboration across diverse departments, sites, contract manufacturers, suppliers, and testing laboratories, nurturing a culture dedicated to continuous quality improvement. By utilizing automated workflows, organizations can not only increase operational efficiency but also enhance risk visibility across products and processes through a holistic risk management approach. The comprehensive suite of quality applications accelerates processes, boosts productivity, and reinforces GxP compliance throughout all operations. Furthermore, Vault QMS ensures the efficient execution of critical quality management tasks, incorporating built-in best practices for managing deviations, performing internal and external audits, handling complaints, conducting lab investigations, overseeing change control, addressing corrective and preventive actions (CAPA), and facilitating quality risk management, ultimately cultivating a resilient quality culture organization-wide. As a result, businesses are empowered to satisfy compliance mandates while simultaneously improving overall productivity and bolstering their reputation within the industry, leading to sustained success and growth. This commitment to quality excellence not only benefits the organizations but also enhances the trust of stakeholders and consumers alike.

What is QbDVision?

QbDVision represents a groundbreaking cloud-enabled platform designed for Digital CMC, with the goal of streamlining the drug development journey by transforming disparate scientific data into valuable process intelligence. This innovative solution enables pharmaceutical and biotechnology teams to methodically collect, organize, and connect product and manufacturing insights throughout the entire development lifecycle, thereby replacing fragmented spreadsheets and conventional document-based methods with an integrated, data-centric framework. The platform's robust architecture provides visibility into all inputs, variables, and objectives associated with development processes, allowing users to evaluate how changes may impact downstream outcomes and overall product quality. By standardizing data using uniform terminologies and contextual frameworks, QbDVision enhances risk-based decision-making, promotes better collaboration among teams, and strengthens their readiness for regulatory compliance. Moreover, this platform equips teams with the tools necessary to navigate the intricacies of drug development, ensuring that informed decisions are made throughout the process. Ultimately, QbDVision not only facilitates efficiency but also fosters innovation in the pharmaceutical landscape.

Media

Media

Integrations Supported

Additional information not provided

Integrations Supported

Additional information not provided

API Availability

API Availability

Pricing Information

Pricing not provided

Pricing Information

Pricing not provided
Free Trial Offered?

Supported Platforms

SaaS

Supported Platforms

SaaS

Customer Service / Support

24 Hour Support

Customer Service / Support

Standard Support
Web-Based Support

Training Options

Documentation Hub
Webinars
Online Training
On-Site Training

Training Options

Documentation Hub
Webinars
Online Training

Company Facts

Organization Name

Veeva Industries

Date Founded

2007

Company Location

United States

Company Website

www.veeva.com/products/vault-qms/

Company Facts

Organization Name

QbDVision

Company Location

United States

Company Website

www.qbdvision.com

Categories and Features

Audit

Compliance Management
Dashboard
Exceptions Management
Issue Management
Multi-Year Planning
Risk Assessment
Workflow Management

Document Control

Archiving & Retention
Automated Routing
Change Management
Compliance Management
Electronic Signature
Escalation Management
Periodic Review
Version Control

Document Management

Collaboration Tools
Compliance Tracking
Document Archiving
Document Assembly
Document Indexing
Document Retention
Electronic Signature
File Recovery
File Type Conversion
Offline Access
Optical Character Recognition
Version Control

Quality Management

Audit Management
Complaint Management
Compliance Management
Corrective and Preventive Actions (CAPA)
Defect Tracking
Document Control
Equipment Management
ISO Standards Management
Maintenance Management
Risk Management
Supplier Quality Control
Training Management

Categories and Features

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