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Kivo

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22 reviews
  • 1 profiles
  • 5 categories
Average star rating
4.9
Serving customers since
2021
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Kivo Reviews

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Marissa B.
08/12/2024
Validated Reviewer
Verified Current User
Review source: Organic

Intuitive document management system that offers so much more

|Kivo
For context, I work in regulatory affairs/regulatory strategy/medical writing at a pharmaceutical company. My job involves regulatory document archiving, writing, and review, as well as planning/assembling submissions to health authorities. Keeping files organized and easy to find is a big deal for me. I have been using Kivo daily for over 2 years to manage 15+ drug development programs. It was extremely easy to learn and very intuitive for a regulatory affairs professional. We implemented Kivo at our small company of 35+ employees, which spans multiple countries and continents. The Kivo system has been easy to use for everyone. Kivo makes the process incredibly easy for file storage, document creation using their eCTD templates, document editing, collaborative authoring/review, submission building, and more, and we love how much it offers under a single vendor/software package. Other roles at my company make use of the eTMF and QMS systems within Kivo, and I'm looking forward to making use of some of the new project management features in Kivo. We rarely have any technical problems with Kivo, but on the rare occasion we do, the customer support team is very quick to respond and resolve the issue. They are always happy to answer any questions or teach me new features that have been added to Kivo. Kivo makes the logistical and administrative aspects of my job easy, especially because it has been so easy for my non-regulatory colleagues to learn and use. I wholeheartedly recommend the Kivo system to any pharmaceutical company looking for ways to get organized and manage quality compliance. With all that Kivo has to offer, I can't imagine using anything else.
Verified User in Pharmaceuticals
AP
Verified User in Pharmaceuticals
08/02/2024
Validated Reviewer
Verified Current User
Review source: Organic

Best system!

|Kivo
Built for the regulatory professional. Compared to other systems I've used, Kivo is more intuitive and customizable. The EDMS functionality is very efficient and the customer support is above and beyond. The new platform for project management has the potential to be a game changer for regulatory submission timelines/document management.
AB
Aaron B.
07/18/2024
Validated Reviewer
Verified Current User
Review source: Organic

Long term user of Kivo

|Kivo
My company has used Kivo and its previous version, Gemstone, for the past 6 years now. The biggest plus for Kivo is its intuitiveness and ease of use. Having used other document repositories/QMS systems before, there is nothing more simple than Kivo. Plus, the customer service is top-notch, whether that is help with handling a task or asking for a new feature to be created, Kivo is very quick to respond and able to build in your requests to their entire system. My company was so pleased with Kivo that we have now rolled out all their systems, regulatory, quality, and clinical, to all our various functions.

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HQ Location:
Portland, US

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What is Kivo?

Kivo is building the infrastructure for GxP compliance in the era of AI-powered drug development. Its unified cloud platform supports Regulatory, Clinical, and Quality operations — including RIM, eTMF, QMS, controlled document management, submission assembly, eCTD lifecycle management, inspection readiness, SOP management, and training management — within a single, audit-ready environment. With Part 11-compliant e-signatures, role-based permissions, continuous validation assurance, and a lossless data model that preserves context from legacy systems, Kivo gives life sciences teams the compliant foundation to reduce operational friction and accelerate time to market. For more information, visit: https://kivo.io/.

Details

Year Founded
2021
Website
kivo.io