Controlled document management with Part-11 Compliant e-Signatures (Docusign included)
Controlled Documents
Process Automation
Project Management
Corporate Documents
Diligence Readiness
Streamline authoring, publishing handoff, and lifecycle management with RIM
Submission Assembly
Project & Dossier Management
Correspondence & Commitments
eCTD Viewing
ICH Document Templates
Cost-effective eTMF for migration, trial management, inspection and storage
Active Trial Management
Site Management
Inspection Readiness
End of Study TMF Transfer
Long-Term TMF Storage
Gain efficient, compliant oversight of internal and external parties with an intelligent QMS
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?
Enhance clinical and regulatory document submission knowledge at your organization with industry-leading resources.
