GRIP serves as a global regulatory intelligence platform that supports the entire lifecycle of medical devices. It provides access to millions of product registrations and regulatory documents, industry standards, and guidelines across over 100 countries. By leveraging AI, GRIP enables companies to track global regulatory trends, streamline processes such as product registration and compliance, and gain insights into clinical trial data. This powerful tool is pivotal for agencies aiming to maintain compliance while accelerating time to market for medical innovations.
Pure Global Core Features
Global regulatory news tracking
Document search and retrieval
AI-powered data analysis
Clinical trials database
Compliance management tools
Pure Global Pro & Cons
The Cons
No direct information about open source availability or accessible software projects.
Pricing details are not explicitly provided on the website.
No mobile or desktop applications linked from the site.
The Pros
Comprehensive global regulatory consulting with presence in over 30 markets.
Integration of AI and data tools to enhance regulatory research and compliance.
End-to-end support covering registration, quality assurance, and local representation.
Expertise in medical device and in vitro diagnostic product regulations.
Personalized solutions for startups, scaleups, and multinational enterprises.