Average Ratings 0 Ratings
Average Ratings 0 Ratings
Description
Enhance your regulatory operations with our comprehensive, all-in-one regulatory information management solution, IQVIA RIM Smart. By alleviating your team's burden from tedious maintenance tasks, they can concentrate on bringing valuable products to market. RIM Smart represents a cutting-edge approach to regulatory information management, designed to accelerate processes, foster collaboration, improve efficiency, and provide greater visibility across your global portfolio, all while optimizing performance and reducing costs. This secure cloud-based platform offers an integrated, holistic, and intelligent method for managing the entire regulatory workflow. The integration with IQVIA’s safety and quality platform will boost performance and offer increased adaptability. By automating manual tasks and enhancing connectivity, you can achieve not only improved efficiency but also significant cost savings, leading to better coordination and visibility across your enterprise. Embrace this transformative system to ensure your regulatory processes are both modern and effective.
Description
ProcEdge Regulatory Information Management System (RIMS) provides companies with a powerful, centralized platform to manage complex regulatory requirements for their entire global product portfolio. Moving away from traditional Excel-based tracking, it offers a single source of truth that connects multiple departments, providing 360-degree visibility and real-time updates on product registration, license maintenance, and post-registration activities. The platform enables detailed planning and tracking of submission timelines tailored to country-specific regulations, helping users meet compliance standards and reduce costly errors. It features configurable data models, automated email notifications, and a robust workflow engine that streamlines query management and response tracking. ProcEdge RIMS complies with global standards like IDMP and regulatory frameworks including GxP, GDPR, and Part 11. By eliminating redundant systems and manual data entry, it significantly reduces operational expenses and accelerates health agency approvals. The system’s audit trails and electronic signature capabilities ensure data integrity and regulatory reliability. Overall, it empowers regulatory professionals to make faster, informed decisions and maintain product marketability efficiently.
API Access
Has API
No
API Access
Has API
No
Screenshots View All
No images available
Integrations
IQVIA
No
Pricing Details
No price information available.
Free Trial
No
Free Version
No
Pricing Details
$300
Free Trial
No
Free Version
No
Deployment
Web-Based
Yes
On-Premises
No
iPhone App
No
iPad App
No
Android App
No
Windows
No
Mac
No
Linux
No
Chromebook
No
Deployment
Web-Based
Yes
On-Premises
Yes
iPhone App
No
iPad App
No
Android App
No
Windows
Yes
Mac
No
Linux
No
Chromebook
No
Customer Support
Business Hours
No
Live Rep (24/7)
No
Online Support
Yes
Customer Support
Business Hours
Yes
Live Rep (24/7)
Yes
Online Support
Yes
Types of Training
Training Docs
No
Webinars
No
Live Training (Online)
Yes
In Person
No
Types of Training
Training Docs
Yes
Webinars
Yes
Live Training (Online)
Yes
In Person
Yes
Vendor Details
Company Name
IQVIA
Country
United States
Website
www.iqvia.com/solutions/integrated-global-compliance/regulatory-compliance/iqvia-rim-smart
Vendor Details
Company Name
Sarjen Systems Pvt Ltd
Founded
1998
Country
India
Website
rims.sarjen.com