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Vodori Platform

Content management and workflow automation for medical, legal, and regulatory review in pharma, device, and diagnostics.

Solution by Vodori
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Overview

Vodori is a content management platform built specifically for life science companies, including pharmaceutical, biotechnology, medical device, and diagnostics organizations. It supports the medical, legal, and regulatory (MLR) review process by providing tools for content creation, approval, distribution, and optimization, with a focus on compliance and real-time collaboration.

The platform is used by over 100 life science teams globally and is designed to meet GxP, quality, and compliance requirements. Vodori is available to organizations across a range of sizes, from emerging companies to mid-market and enterprise teams, and serves sectors including nutrition and animal health in addition to pharma and medical devices.

Content Creation and Approval

  • Workflow management: Manages promotional and medical content review workflows, enforces compliance requirements, and supports real-time collaboration among reviewers.
  • Claims and evidence management: Allows teams to substantiate materials using independently approved claims and references, linking evidence directly to content.
  • Digital asset management: Serves as a central source of truth for compliant, on-brand materials, ensuring teams access approved assets.
  • Web annotation: Enables reviewers to annotate and collaborate on digital content in its native format, without requiring file conversion or downloads.

Content Distribution

  • Health authority submission support: Assists teams in preparing materials for health authority submissions, including FDA 2253 filings.
  • Portals: Provides filtered access to approved, curated content for specific audiences or teams.
  • Cross-channel publishing: Allows approved content to be published from a single central, controlled location across multiple channels.
  • Global commercialization: Supports sharing and distribution of content across global affiliates.
  • Vodori for Salesforce: Delivers MLR-approved materials directly into Salesforce Life Sciences, Sales, and Service Clouds.

Optimization and Analytics

  • Reporting and analytics: Provides performance metrics and benchmarking data to help teams optimize productivity and content effectiveness.
  • Vodori 360 Customer Program: A customer success program staffed by industry and process experts, designed to deliver value beyond the software itself through ongoing support and guidance.

Compliance and Security

  • The platform is purpose-built to meet GxP, quality, and compliance requirements relevant to life science organizations.
  • Includes enterprise-grade privacy and security features designed for the life sciences industry.

Vodori integrates with third-party systems including Salesforce, IQVIA OCE, and Seismic, allowing organizations to connect the platform into their existing commercial ecosystems. The platform's customer program, Vodori 360, supplements the software with industry expertise and process support.

Meta

Domain
Commercial & Medical Affairs
Subdomain
Medical Affairs Operations
Software type(s)
Workflow Automation
Deployment type(s)
Cloud / SaaS
Industry vertical(s)
BiotechDiagnostics / IVDMedical DevicesPharma
Development stage(s)
ClinicalPost-Market & RWE
Target user(s)
QA / Regulatory AffairsMedical Affairs ProfessionalCommercial / Market Access
Compliance standard(s)
GxP