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Description
Kivo offers an innovative solution for sponsors and CROs, providing an economical document and process management platform that enables life sciences teams to efficiently accomplish their tasks within a single, user-friendly, and compliant environment. By integrating DMS, RIM, QMS, eTMF, and eCTD functionalities, Kivo allows teams in pharmaceuticals, biotechnology, medical devices, and biologics to handle regulated documents, quality management activities, clinical trial documentation, regulatory submissions, and workflow processes without the hassle of using multiple disconnected tools. With Kivo’s Document Management System, users can manage controlled documents and automate processes while ensuring project oversight, corporate documentation, and readiness for due diligence in a centralized manner, featuring version control, collaboration tools, audit trails, search capabilities, workflow automation, and Part 11-compliant electronic signatures. Additionally, the RIM system enhances project management and correspondence, facilitates submission building and publishing handoff, provides eCTD viewing options, and streamlines dossier management and interactions with health authorities. Overall, Kivo equips life sciences teams with the necessary tools to maintain compliance and efficiency in their operations.
Description
In the rapidly evolving world of regulatory requirements, Titanium presents an all-encompassing array of applications specifically designed to ensure that your sample management program remains compliant, efficient, and streamlined. Discover the exceptional advantages of our SaaS platform, which leverages cloud technology to provide innovative solutions that adhere to both PDMA and 21 CFR Part 11 standards. With a versatile suite of applications, Titanium effectively tackles various compliance hurdles while ensuring smooth interoperability, thus delivering a holistic and cohesive approach to meet your compliance demands. Our platform is engineered to adapt as your business expands, guaranteeing that each data entry is singular and universally accessible across all applications. Enhance transparency and accountability with integrated audit trails that facilitate effortless tracking and reporting. As a well-established application, Titanium continually advances through regular updates, ensuring that you remain at the cutting edge of compliance technology. Furthermore, we prioritize user feedback to adapt and refine our offerings, empowering clients to navigate the complexities of compliance with confidence.
API Access
Has API
API Access
Has API
Pricing Details
$1,800 per month
Free Trial
Free Version
Pricing Details
No price information available.
Free Trial
Free Version
Deployment
Web-Based
On-Premises
iPhone App
iPad App
Android App
Windows
Mac
Linux
Chromebook
Deployment
Web-Based
On-Premises
iPhone App
iPad App
Android App
Windows
Mac
Linux
Chromebook
Customer Support
Business Hours
Live Rep (24/7)
Online Support
Customer Support
Business Hours
Live Rep (24/7)
Online Support
Types of Training
Training Docs
Webinars
Live Training (Online)
In Person
Types of Training
Training Docs
Webinars
Live Training (Online)
In Person
Vendor Details
Company Name
Kivo
Founded
2021
Country
United States
Website
kivo.io
Vendor Details
Company Name
QPharma
Country
United States
Website
qpharmacorp.com/products/titanium/
Product Features
Document Management
Access Controls
Archiving & Retention
Collaboration Tools
Compliance Tracking
Document Archiving
Document Assembly
Document Capture
Document Conversion
Document Delivery
Document Indexing
Document Retention
Electronic Signature
Email Management
File Recovery
File Type Conversion
Forms Management
Full Text Search
Offline Access
Optical Character Recognition
Print Management
Version Control