Establish clear, compliant content management practices with Vodori
With Vodori, emerging life science companies establish clear and compliant content management practices–increasing speed-to-market of critical communications before, during, and after their first product launch.
Optimize how your MLR/PRC teams collaborate to review and approve content by establishing a clear process early. Start with corporate, medical, or scientific materials and hit the ground running when you’re ready to distribute commercial content.
Launch faster
The time leading up to a product launch is hectic. Having a solid process in place to review, approve, and distribute your commercial content as soon as you receive regulatory approval makes the race to the finish line that much easier.
Align with regulations
Have confidence that you’re operating in a fully compliant manner from the start. When you submit to a regulatory body like the FDA, you’ll be prepared thanks to a system that automates and tracks key processes and content lifecycle stages.
Vodori's user-friendly interface enables your team to collaborate on corporate, medical, and commercial content reviews quickly–putting more time back in their day to focus on other projects. For a growing company who needs to quickly onboard new employees, it’s important to choose an MLR solution that will enable easy adoption of the technology as review accountability shifts and changes.
New users get started with just one 60 minute training
Designed with UX and UI best practices
Modern MLR solution with features purpose-built for life sciences
Our team is known for being responsive and a true partner for all customers, regardless of size. As you experience growth and change, the Vodori team will assist by advising on best practices, answering questions, and making any configuration changes to our software to align with your new business needs at no additional charge. We’re here to anticipate your needs and ensure you’re successful with our products.
Vodori automates compliance through configurable workflows and serves as one source of truth for your commercial content. Vodori is also a validated system with SOC 2 Type II attestation. Our rigorous compliance program covers data security, SDLC and infrastructure, risk management, and more, so as your company matures, we have you covered.
e-Signatures in compliance with 21 CFR Pt 11 & EU Annex 11
At your size, you don’t have time for a drawn out implementation project. Emerging life science companies can get up and running with Vodori in as little as one week. Every part of the implementation process–from kickoff to training and launch–is handled by the Vodori team.
Get up and running in as little as one week
Minimal time investment from your team
Industry standard workflows
Easy to learn and use
Vodori's user-friendly interface enables your team to collaborate on corporate, medical, and commercial content reviews quickly–putting more time back in their day to focus on other projects. For a growing company who needs to quickly onboard new employees, it’s important to choose an MLR solution that will enable easy adoption of the technology as review accountability shifts and changes.
New users get started with just one 60 minute training
Designed with UX and UI best practices
Modern MLR solution with features purpose-built for life sciences
Expert attention from customer success
Our team is known for being responsive and a true partner for all customers, regardless of size. As you experience growth and change, the Vodori team will assist by advising on best practices, answering questions, and making any configuration changes to our software to align with your new business needs at no additional charge. We’re here to anticipate your needs and ensure you’re successful with our products.
Ongoing access to our Customer Success Team
Advice on SOPs and industry best practices
24/7 global support
Compliance for today… and tomorrow
Vodori automates compliance through configurable workflows and serves as one source of truth for your commercial content. Vodori is also a validated system with SOC 2 Type II attestation. Our rigorous compliance program covers data security, SDLC and infrastructure, risk management, and more, so as your company matures, we have you covered.
e-Signatures in compliance with 21 CFR Pt 11 & EU Annex 11
Downloadable audit trail
FDA submission package
Fast, simplified implementations
At your size, you don’t have time for a drawn out implementation project. Emerging life science companies can get up and running with Vodori in as little as one week. Every part of the implementation process–from kickoff to training and launch–is handled by the Vodori team.
Get up and running in as little as one week
Minimal time investment from your team
Industry standard workflows
“We chose Vodori at Orphazyme because the offering is relevant, their size is attractive, their price is competitive, and their responsiveness has been excellent. It was the right choice for us as an emerging ultra-rare company.”
Patrick Lennon VP, Analytics & Operations, Orphazyme
Contact our Sales team to discuss your regulated content management needs. For additional life science resources–such as ebooks and white papers–visit our resources hub.
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