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Ratings and Reviews 0 Ratings
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What is Zelthy Regulatory Affairs?
Zelthy Regulatory Affairs is an innovative software solution tailored for teams in the pharmaceutical and biotechnology industries, streamlining the management of submissions to multiple health authorities and regulatory bodies. It provides a detailed overview of submission pipelines, essential milestones, jurisdiction-specific requirements, and health authority inquiries. The platform enables teams to systematically arrange regulatory dossiers, validate publishing packages, coordinate the review process, and oversee post-approval variations and labeling changes. In addition, regulatory intelligence features are included to track updates in guidelines and requirements, assess their impact on portfolios, and uncover any gaps in dossier preparedness. Enhanced by AI capabilities, it assists in the creation of documents and the drafting of materials needed for regulatory evaluations. Moreover, Zelthy integrates seamlessly with enterprise systems like Veeva RIM and offers deployment options that include cloud, on-premises, or hybrid solutions, ensuring adaptability to meet diverse organizational needs. This all-encompassing approach not only enhances efficiency but also supports regulatory teams in maintaining compliance, making Zelthy an indispensable tool in their operational arsenal. With a focus on continuous improvement and innovation, Zelthy empowers organizations to navigate the complex regulatory landscape effectively.
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.
Integrations Supported
Adobe Acrobat Sign
Amazon Web Services (AWS)
Docusign
Google Workspace
Microsoft 365
Microsoft Azure
NiCE CXone Mpower
Salesforce
Snowflake
TraceLink
API Availability
Has API
API Availability
Pricing Information
Pricing not provided
Pricing Information
Pricing not provided
Supported Platforms
SaaS
On-Prem
Supported Platforms
SaaS
Customer Service / Support
Web-Based Support
Customer Service / Support
Standard Support
Web-Based Support
Training Options
Not specified
Training Options
Documentation Hub
Webinars
Online Training
On-Site Training
Company Facts
Organization Name
Healthlane Technologies
Date Founded
2017
Company Location
India
Company Website
www.zelthy.com/solutions/regulatory
Company Facts
Organization Name
Arazy Group
Company Location
Canada
Company Website
arazygroup.com/regislate-software/
Categories and Features
Regulatory Information Management (RIM)
Not specified
Categories and Features
Regulatory Information Management (RIM)
Not specified