Unite Clinical, Regulatory, and Quality teams in one simple, compliant workspace.
Cost-effective eTMF solutions for trial management, migration, inspection and storage
Streamline authoring, publishing handoff, and lifecycle management with RIM
Gain efficient, compliant oversight of internal and external parties with an intelligent QMS
Add over 450 pre-formatted templates for ICH, FDA, EMA, Health Canada and more.
Kivo offers solutions for Clinical, Regulatory, and Quality use cases. Unsure what you need? Talk to our team and try Kivo free for 30 days.
Active Trial Management
Site Management
Inspection Readiness
End of Study TMF Transfer
Long-Term TMF Storage
Correspondence & Commitments
Submission Assembly
ICH Document Templates
Project & Dossier Management
eCTD Viewing
CAPA Management
Vendor Audits
SOP & Training Management
Access our whitepapers, case studies, webinars, demos, and articles - all in one place
The latest news and insights from our team, from industry news to product feature updates
Kivo partners with a variety of organizations across the Life Sciences industry
Hear our story and learn what drives us
Security & Compliance at Kivo
Interested in working for Kivo? View job postings
How can we help?