PureID - A global AI empowered life science service provider

Relying on a global expert service team with extensive regulatory certification and clinical experience, PureID provides full-process consulting and overseas clinical research trial services for medical devices, in-vitro diagnostics, medical software AI, and other products to achieve global market compliance. By leveraging digital technology to empower medical compliance and clinical trials, we disrupt traditional and conventional methods, making medical device exportation more one-stop and intelligent.

GRIP - Global Regulatory Intelligence Platform

Empowering the entire lifecycle of medical devices globally with AI, we are the best partner for medical device manufacturers expanding overseas.

AI-empowered, automatically generated regulatory document services

Taking the lead in introducing AI technology in the industry, significantly improving work efficiency. Taking the automatic generation of product instructions (IFU) as an example, you only need to input the product name, company name, company logo, and language to quickly generate documents.

Medical device R&D stage

Pure Radar - GRIP compiles and collects regulatory news updates on medical devices from over 35 major countries and regions, as well as complete documents on 100+ regulatory laws, regulations, and directives related to medical devices from various countries and regions. It provides a one-stop-shop for obtaining access to the latest and most authoritative global regulatory information on product medical registration processes.
Pure Trials - GRIP compiles clinical trial registration data from various countries and regions around the world, with over 1 million clinical trial registration data now included. It provides advanced filtering options and beautiful data visualization charts, helping medical device manufacturers quickly understand and keep up with the latest medical research and development directions and fields internationally.

Medical device registration stage

Pure Cert - Centralized management of product registration, related certificates, and local agents, with built-in management for medical device registration and related certificates in 34 countries including the United States, Europe, and Australia. The intelligent reminder function allows you to anticipate changes in compliance status in advance, plan ahead, and gain an advantage.
Pure Meta - GRIP collects medical device registration data from major countries and regions around the world, with a total of over 3 million product registration-related data. This includes medical device registration data from countries and regions such as the United States FDA, the European Union, Australia, the United Kingdom, China, South Korea, Japan, Canada, and Singapore. Its powerful intelligent comparison algorithm allows you to quickly find the most suitable reference products for comparison.
Biobank - Our company has a total of 6 biobanking projects worldwide that are currently collecting various types of samples on an ongoing basis. Additional resources are being approached to help us both expand our operations both horizontally and vertically in terms of numbers of samples and sample types.

Medical device market launch stage

Pure Markets - Covering over 40 countries with a total of more than 600,000 medical device distributor data and WHO tendering data, we help you complete the 'last mile' of going global, allowing medical products to quickly reach the world.

This application is available in Chinese and English.

GRIP - Global Regulatory Intelligence Platform普瑞纯证医疗科技（广州）有限公司

GRIP - Global Regulatory Intelligence Platform

普瑞纯证医疗科技（广州）有限公司

GRIP - Global Regulatory Intelligence Platform

普瑞纯证医疗科技（广州）有限公司

GRIP - Global Regulatory Intelligence Platform
普瑞纯证医疗科技（广州）有限公司