Ratings and Reviews 0 Ratings
Ratings and Reviews 0 Ratings
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What is PhlexRIM?
PhlexRIM promises to greatly improve compliance by offering instantaneous access to worldwide registration data in a remarkably efficient way. The newest iteration, PhlexRIM 2.0, introduces a suite of pre-configured automation assistants, referred to as "bots," along with regulatory scenarios that comply with industry standards. Its user-friendly drag-and-drop design interface empowers regulatory teams to optimize their workflows without the necessity for programming knowledge or IT support. Moreover, it efficiently manages the lifecycle of pharmaceutical product registration, allowing users to obtain comprehensive status updates and utilize the alert management system embedded in all processes. The reporting functions are extensive, providing options for both standard reports and the ability to craft custom reports that meet specific requirements. Furthermore, the platform supports the development and delegation of regulatory tasks across multiple organizational levels, including management, departments, headquarters, and affiliates, fostering effective teamwork and collaboration among diverse teams. This comprehensive functionality positions PhlexRIM 2.0 as a crucial tool for regulatory compliance and operational efficiency in the pharmaceutical sector.
What is Kivo?
Kivo presents a groundbreaking solution tailored for sponsors and CROs by offering an affordable document and process management platform that empowers life sciences teams to effectively execute their responsibilities in a cohesive, user-friendly, and compliant setting. By combining functionalities such as DMS, RIM, QMS, eTMF, and eCTD, Kivo enables professionals in the pharmaceutical, biotechnology, medical device, and biologics sectors to manage regulated documentation, quality assurance tasks, clinical trial records, regulatory submissions, and workflow processes seamlessly, eliminating the complications associated with juggling multiple disconnected tools. With its Document Management System, Kivo allows users to oversee controlled documents and automate workflows, ensuring project monitoring, corporate documentation management, and due diligence preparedness in a streamlined manner through features like version control, collaborative tools, audit trails, robust search capabilities, workflow automation, and Part 11-compliant electronic signatures. Furthermore, the RIM component significantly enhances project oversight and communication, simplifies submission construction and publishing transitions, offers eCTD viewing alternatives, and optimizes dossier management and interactions with regulatory bodies. Overall, Kivo equips life sciences teams with essential tools that ensure compliance and boost operational efficiency, ultimately leading to improved project outcomes and a more organized workflow. This comprehensive approach not only addresses current challenges but also prepares organizations for future demands in the rapidly evolving life sciences landscape.
Integrations Supported
Integrations Supported
Docusign
Gmail
Jama Connect
Jira
Microsoft 365
Microsoft 365 Copilot
Microsoft Excel
Microsoft SharePoint
Microsoft Word
API Availability
API Availability
Has API
Pricing Information
Pricing not provided
Pricing Information
Pricing not provided
Supported Platforms
SaaS
Supported Platforms
SaaS
Customer Service / Support
Standard Support
Web-Based Support
Customer Service / Support
Web-Based Support
Training Options
Documentation Hub
Webinars
Online Training
Training Options
Documentation Hub
Online Training
Company Facts
Organization Name
Phlexglobal
Date Founded
1997
Company Location
United Kingdom
Company Website
www.phlexglobal.com/phlexrim
Company Facts
Organization Name
Kivo
Date Founded
2021
Company Location
United States
Company Website
kivo.io
Categories and Features
Regulatory Information Management (RIM)
Not specified
Submission Management
Not specified
Categories and 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
Print Management
Version Control
Life Sciences
Not specified
Medical Quality Management Systems
Not specified
Pharmaceutical and Biotech
Not specified
Regulatory Information Management (RIM)
Not specified