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What is Regislate?

Acquire all essential tools to successfully register your medical device or IVD product in international markets while managing your market access license throughout its entire life cycle. REGISLATE® provides users with detailed submission file requirements customized for distinct medical and IVD device specifications in various countries. This platform allows you to track milestones, timelines, and both estimated and actual completion dates for initial registrations, renewals, amendments, and license transfers in real-time. In addition, it presents infographic data and unique indicators to support clear oversight and management of each project. Utilize collaborative features that aid in the preparation and evaluation of submissions, ensuring adherence to all critical requirements and documentation. Stay updated with real-time reports on both ongoing and future submissions, complete with insights into market access preparedness. Furthermore, REGISLATE® includes GR-MAP registration tracking, which offers comprehensive visibility regarding both the country and product involved. This integrated strategy guarantees that users are thoroughly prepared to skillfully navigate the intricate landscape of market access, ultimately enhancing efficiency and compliance throughout the process. Regular updates and user-friendly navigation further enrich the experience, making it an invaluable resource for professionals in the industry.

What is IQVIA RIM Smart?

Transform your regulatory operations with our innovative regulatory information management solution, IQVIA RIM Smart. By relieving your team of monotonous maintenance duties, they can focus on introducing essential products to the market more swiftly. RIM Smart embodies a state-of-the-art methodology for managing regulatory information, aimed at expediting processes, promoting collaboration, enhancing efficiency, and offering improved transparency across your international portfolio while optimizing performance and curtailing expenses. This secure, cloud-based platform delivers an integrated, comprehensive, and intelligent approach to oversee the complete regulatory workflow. The synergy with IQVIA’s safety and quality platform will elevate performance and enhance flexibility in your operations. Through the automation of manual tasks and improved connectivity, your organization can not only experience increased efficiency but also achieve notable cost reductions, resulting in superior coordination and oversight across your operations. Adopting this groundbreaking system will ensure that your regulatory procedures are both contemporary and highly effective, ultimately positioning your organization for future success. With RIM Smart, you can navigate regulatory landscapes with confidence and ease.

Media

Media

Integrations Supported

IQVIA

Integrations Supported

IQVIA

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

Arazy Group

Company Location

Canada

Company Website

arazygroup.com/regislate-software/

Company Facts

Organization Name

IQVIA

Company Location

United States

Company Website

www.iqvia.com/solutions/integrated-global-compliance/regulatory-compliance/iqvia-rim-smart

Categories and Features

Categories and Features

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