Res_Q

Res_Q

Sware
+
+

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About

Kivo is a better way to work for sponsors and CROs, offering an affordable document and process management system that helps life sciences teams get work done in one intuitive, compliant workspace. It brings DMS, RIM, QMS, eTMF, and eCTD capabilities together so pharmaceutical, biotech, medical device, and biologics teams can manage regulated documents, quality activities, clinical trial files, regulatory submissions, and process workflows without disconnected tools. Kivo’s Document Management System provides one place for controlled documents, process automation, project management, corporate documents, and diligence readiness, with centralized storage, version control, collaboration, audit trails, search, workflow automation, and Part 11-compliant e-signatures. Its RIM system supports correspondence, project management, submission building, publishing handoff, eCTD viewing, dossier management, agency interactions, health authority commitments, etc.

About

Meet the leading-edge validation solution that automates, unifies, and accelerates your success. Res_Q helps IT and quality leaders eliminate validation debt, achieve peace of mind, and untangle valuable resources. Res_Q’s data-focused architecture and a wide array of industry-supported applications prevent you from falling deeper into validation debt with every new software release. The open API approach unlocks a bi-directional data flow that empowers system integrations, migration during onboarding, and more. Configurable workflows to both match your operational requirements and integrate industry best practices. All validation processes are controlled in a single system, serving all areas across the enterprise, including IT, manufacturing, lab systems, and more. Initiate workflows and assign workloads based on risk profile. Res_Q puts quality at the forefront without sacrificing speed.

Platforms Supported

Windows
Mac
Linux
Cloud
On-Premises
iPhone
iPad
Android
Chromebook

Platforms Supported

Windows
Mac
Linux
Cloud
On-Premises
iPhone
iPad
Android
Chromebook

Audience

Growing biotech regulatory teams that need compliant document management, quality workflows, submission planning, and clinical trial file control in one validated life sciences platform

Audience

Organizations wanting a tool to reduce costs, prevents adoption delays, and streamlines cumbersome compliance requirements

Support

Phone Support
24/7 Live Support
Online

Support

Phone Support
24/7 Live Support
Online

API

Offers API

API

Offers API

Screenshots and Videos

Screenshots and Videos

Pricing

$1,800 per month
Free Version
Free Trial

Pricing

No information available.
Free Version
Free Trial

Reviews/Ratings

Overall 0.0 / 5
ease 0.0 / 5
features 0.0 / 5
design 0.0 / 5
support 0.0 / 5

This software hasn't been reviewed yet. Be the first to provide a review:

Review this Software

Reviews/Ratings

Overall 0.0 / 5
ease 0.0 / 5
features 0.0 / 5
design 0.0 / 5
support 0.0 / 5

This software hasn't been reviewed yet. Be the first to provide a review:

Review this Software

Training

Documentation
Webinars
Live Online
In Person

Training

Documentation
Webinars
Live Online
In Person

Company Information

Kivo
Founded: 2021
United States
kivo.io

Company Information

Sware
United States
www.sware.com/solutions/platform

Alternatives

Alternatives

Tricentis Vera

Tricentis Vera

Tricentis
BeeCTD

BeeCTD

Altamira
LifeSphere RIMS

LifeSphere RIMS

ArisGlobal

Categories

Categories

Integrations

Docusign
Adobe Acrobat Sign
Amazon Web Services (AWS)
Benchling
Box
Gmail
LabVantage
LabWare LIMS
Microsoft Dynamics 365
NetSuite
Nuvolo
Okta
OpenClinica
SAP Cloud Platform
ServiceNow
Smartsheet
TraceLink
TrackWise
Veeva CRM
ZenQMS

Integrations

Docusign
Adobe Acrobat Sign
Amazon Web Services (AWS)
Benchling
Box
Gmail
LabVantage
LabWare LIMS
Microsoft Dynamics 365
NetSuite
Nuvolo
Okta
OpenClinica
SAP Cloud Platform
ServiceNow
Smartsheet
TraceLink
TrackWise
Veeva CRM
ZenQMS
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