Company profile
Kivo
The GxP Compliant, agent-native platform for Regulatory, Clinical, and Quality operations. Makers of Headless GxP
- Industry
- Software Development
- Employees
- 46
- Headquarters
- Portland, Oregon
- Founded
- 2021
- LinkedIn followers
- 1,730
- Office locations
- 1
Kivo company summary
Kivo is a company in the Software Development industry, headquartered in Portland, Oregon, founded in 2021. On LinkedIn the company has around 46 employees and 1,730 followers. Its listed specialties include Regulatory, Clinical, Quality, Regulatory Submissions, eCTD Templates.
What technology does Kivo use?
No technologies detected yet. Warmrank rechecks company websites on a rolling basis.
About 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. Clinical Capabilities: eTMF - Electronic Trial Master File TMF Transfer & Migration Trial Archiving / Long Term Storage Active CRO Trial Management Vendor Management Inspection Preparedness & Readiness Regulatory Capabilities: RIM - Regulatory Information Management eCTD - Electronic Common Technical Document Submission Assembly Document Templates Project Management Registration Management Dossier Management Quality Capabilities: QMS - Quality Management System CAPA Management Vendor Audit SOP Management Training
Specialties
Where is Kivo located?
Kivo lists 1 location.
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|---|---|---|---|---|
Kivo kivo.io | Software Development | 46 | 2021 | Portland, Oregon |
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Frequently asked questions about Kivo
What does Kivo do?
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. Clinical Capabilities: eTMF - Electronic Trial Master File TMF Transfer & Migration Trial Archiving / Long Term Storage Active CRO Trial Management Vendor Management Inspection Preparedness & Readiness Regulatory Capabilities: RIM - Regulatory Information Management eCTD - Electronic Common Technical Document Submission Assembly Document Templates Project Management Registration Management Dossier Management Quality Capabilities: QMS - Quality Management System CAPA Management Vendor Audit SOP Management Training
How many employees does Kivo have?
Kivo has around 46 employees on LinkedIn.
Where is Kivo headquartered?
Kivo is headquartered in Portland, Oregon.
When was Kivo founded?
Kivo was founded in 2021.
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