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What is Samarind RMS?
Samarind RMS presents an advanced approach to managing your medical product information with greater efficiency. By utilizing Samarind RMS, users can enter data a single time and leverage it multiple times as necessary. For example, an 'INN' can be recorded once and subsequently used for all relevant IMA submissions, renewals, variations, PSURs, and XEVMPD processes. This concept applies to all critical data within the system, which has proven to boost workflow efficiency and enhance data quality significantly. Our user-friendly approach to system design and execution enables clients to manage their licenses effortlessly and with assurance, as our single-source-of-truth™ method for regulatory affairs professionals delivers a thorough end-to-end solution. Furthermore, our platform features an electronic document management system (EDMS) that includes version control, template creation, and the ability to integrate with external document management solutions like Documentum™ or SharePoint™, facilitating a smooth incorporation of all your documentation requirements. Ultimately, Samarind RMS not only enables users to handle their information effectively but also fosters improved collaboration among various departments, thereby enhancing overall operational productivity. This comprehensive capability makes it a valuable asset for any organization in the medical field.
What is RIMTrack?
As national regulations continue to change rapidly and the complexities of regulatory submissions grow, healthcare and life sciences companies are placing greater emphasis on implementing advanced methodologies and intelligent systems designed to boost efficiency, cut costs, and accelerate submission processes. In addressing these challenges, RIMTrack stands out as an innovative regulatory information management solution that harnesses the power of cloud-based artificial intelligence. Created with a focus on supporting organizations in achieving accurate and effective submission preparations, it also streamlines the various regulatory processes associated with tracking, licensing, approvals, competitive intelligence, clinical trials, and comprehensive reporting to international stakeholders. RIMTrack's ability to integrate smoothly with current Regulatory Information Management systems allows for a comprehensive, end-to-end management of the entire regulatory lifecycle, equipping organizations to handle compliance complexities with increased ease and precision. These technological advancements not only enhance operational efficiency but also enable organizations to more swiftly adapt to evolving regulatory landscapes, ensuring they remain competitive and compliant in the long run. As such, the implementation of RIMTrack signifies a strategic investment in future-proofing regulatory processes.
Integrations Supported
Microsoft 365
Microsoft Azure
Microsoft Dynamics 365
Microsoft SharePoint
OpenText Documentum
Integrations Supported
Microsoft 365
Microsoft Azure
Microsoft Dynamics 365
Microsoft SharePoint
OpenText Documentum
API Availability
Has API
API Availability
Has API
Pricing Information
Pricing not provided.
Free Trial Offered?
Free Version
Pricing Information
Pricing not provided.
Free Trial Offered?
Free Version
Supported Platforms
SaaS
Android
iPhone
iPad
Windows
Mac
On-Prem
Chromebook
Linux
Supported Platforms
SaaS
Android
iPhone
iPad
Windows
Mac
On-Prem
Chromebook
Linux
Customer Service / Support
Standard Support
24 Hour Support
Web-Based Support
Customer Service / Support
Standard Support
24 Hour Support
Web-Based Support
Training Options
Documentation Hub
Webinars
Online Training
On-Site Training
Training Options
Documentation Hub
Webinars
Online Training
On-Site Training
Company Facts
Organization Name
Instem
Date Founded
1969
Company Location
United States
Company Website
www.instem.com/solutions/samarind-rms/
Company Facts
Organization Name
WinWire Technologies
Company Location
United States
Company Website
www.winwire.com/regulatory-information-management/