Audience
Healthcare providers and clinical professionals looking for a global medtech registration management solution
About Regislate
Everything you need to successfully register your medical device or IVD product in any market around the world and manage your market access license through the product life cycle. REGISLATE® provides users with medical and IVD device-specific at country-specific complete submission file requirements. Users can manage milestones, timelines and estimated and actual completion dates for initial registrations, renewals, amendments and license transfers in real-time. Infographic data and proprietary indicators for clear monitoring and management of each project are available. Utilize collaboration tools for preparation and review of submissions, compliance requirements and documents. Recieve progress reports in real-time for current and future submissions including market access readiness index. REGISLATE® includes GR-MAP registration tracking for both country and product.
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Integrations
No integrations listed.
Company Information
Arazy Group
Canada
arazygroup.com/regislate-software/
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Product Details
Platforms Supported
Cloud
Training
Documentation
Live Online
Webinars
In Person
Support
Phone Support
Online
Regislate Frequently Asked Questions
Q: What kinds of users and organization types does Regislate work with?
Regislate works with these users and organization types: Mid Size Business, Small Business, Enterprise, Freelance, Nonprofit, Government, and Startup.
Q: What languages does Regislate support in their product?
Regislate supports these languages: English.
Q: What kind of support options does Regislate offer?
Regislate offers support via phone support and online.
Q: What type of training does Regislate provide?
Regislate provides training in the form of documentation, live online, webinars, and in person.
