Biotech & pharmaceutical content management solutions
Vodori is specifically designed to help life sciences teams achieve speed and compliance.
View Platform OverviewA modern approach to regulated content management
If your generic or legacy content management systems make it hard to get content to market, launch campaigns, respond to market conditions, and maintain compliance–it’s time to rethink your solutions. Vodori is a modern, validated platform built exclusively to reduce risk and streamline the review, approval, and distribution processes for pharmaceutical and biotech organizations.
Modern, turnkey regulated content management
Review and approve content up to 80% faster
Our solutions are designed to be incredibly easy to use. Your review team can log in, review, collaborate on, and approve content quickly to support product launches and respond to needs in the field.
Automate and streamline compliance
Automatically capture key compliance information like an audit trail and 21 CFR Pt 11 eSignature to streamline operations. Facilitate effective review processes with claims management, version history, FDA submission package, and more.
Deliver compliant, approved content to sales and MSLs
As content is reviewed, approved, modified, or expired it is automatically updated in the digital asset management module or your downstream system of choice. This ensures compliant content usage based on user permissions–such as region, product, role, or disease state.
Optimize processes with data
Leverage process KPIs like average review time, circulations, task time by user, and more to make informed decisions about your people, processes, and technology. We’ll be there to help you dissect and apply insights every step of the way.
Backed by a team of experts
Every Vodori customer receives 24/7/365 end user support and access to our Customer Success Team to ensure your success with our software. We’ll share best practices, provide process consultation, and work with you to make modifications needed as your business grows and changes.
Review and approve content up to 80% faster
Our solutions are designed to be incredibly easy to use. Your review team can log in, review, collaborate on, and approve content quickly to support product launches and respond to needs in the field.
Automate and streamline compliance
Automatically capture key compliance information like an audit trail and 21 CFR Pt 11 eSignature to streamline operations. Facilitate effective review processes with claims management, version history, FDA submission package, and more.
Deliver compliant, approved content to sales and MSLs
As content is reviewed, approved, modified, or expired it is automatically updated in the digital asset management module or your downstream system of choice. This ensures compliant content usage based on user permissions–such as region, product, role, or disease state.
Optimize processes with data
Leverage process KPIs like average review time, circulations, task time by user, and more to make informed decisions about your people, processes, and technology. We’ll be there to help you dissect and apply insights every step of the way.
Backed by a team of experts
Every Vodori customer receives 24/7/365 end user support and access to our Customer Success Team to ensure your success with our software. We’ll share best practices, provide process consultation, and work with you to make modifications needed as your business grows and changes.
“My experience working with Vodori felt like a real partnership. Vodori is responsive and really understands our needs.”
Associate Director Sales and Marketing, US pharmaceutical company
Compare Vodori to other solutions
Vodori comes with turnkey implementation, transparent pricing, and an accelerated time to value. Get a more in-depth comparison to Veeva PromoMats here.
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